Paracetamol (N-acetyl-p-aminophenol (APAP), otherwise known as acetaminophen) is the active ingredient in more than 600 medications used to relieve mild to moderate pain and reduce fever. APAP is widely used by pregnant women as governmental agencies, including the FDA and EMA, have long considered APAP appropriate for use during pregnancy when used as directed. However, increasing experimental and epidemiological research suggests that prenatal exposure to APAP might alter fetal development, which could increase the risks of some neurodevelopmental, reproductive and urogenital disorders. Here we summarize this evidence and call for precautionary action through a focused research effort and by increasing awareness among health professionals and pregnant women. APAP is an important medication and alternatives for treatment of high fever and severe pain are limited. We recommend that pregnant women should be cautioned at the beginning of pregnancy to: forego APAP unless its use is medically indicated; consult with a physician or pharmacist if they are uncertain whether use is indicated and before using on a long-term basis; and minimize exposure by using the lowest effective dose for the shortest possible time. We suggest specific actions to implement these recommendations. This Consensus Statement reflects our concerns and is currently supported by 91 scientists, clinicians and public health professionals from across the globe.
A growing body of experimental and epidemiological research suggests that prenatal exposure to paracetamol (N-acetyl-p-aminophenol (APAP), otherwise known as acetaminophen) might alter fetal development, which could in turn increase the risks of certain neurodevelopmental, reproductive and urogenital disorders1,2,3. APAP is the active ingredient in more than 600 prescription and non-prescription medications used to relieve mild to moderate pain and reduce fever (Consumer Health Products Association — acetaminophen). Sales of APAP-containing products, which are not restricted to pharmacies in many countries, are increasing worldwide4. Adverse effects of APAP are well known; for example, intentional overdose, unintentional overdose5,6 and chronic use have resulted in APAP being the leading cause of acute liver failure in children7 and adults5,8 in the Western world. Of note, APAP is widely used by pregnant women, as the FDA and EMA have long considered APAP-containing products to be of minimal risk when used as directed during pregnancy9,10.
As scientists, medical experts and public health professionals, we are concerned about increasing rates of neurological, urogenital and reproductive disorders. We are witnessing disturbing increases in the number of children with cognitive, learning and/or behavioural problems. For example, the US National Health Interview Survey reported that between 2009 and 2017, approximately one in six children aged 3–17 years had a developmental disability diagnosis. A 9.5% increase was observed in the overall rate of developmental disabilities between 2009–2011 and 2015–201711.
Furthermore, in Western regions the prevalence of male reproductive and urogenital disorders has increased. These disorders include cryptorchidism, hypospadias and testicular germ cell cancer, together with early puberty, decreased sperm counts, levels of sex hormones and decreased fertility12,13. Data support the contribution of environmental exposure during fetal life, including exposure to pharmaceuticals, to these increases in rates of neurological, urogenital and reproductive disorders13,14.
In this Consensus Statement, we summarize the epidemiological research and animal studies that have examined neurological, urogenital and reproductive outcomes that have been associated with maternal and perinatal use of APAP (Figs 1,2). Based on this research, we believe we know enough to be concerned about the potential developmental risks associated with prenatal APAP exposure and therefore call for precautionary action. We provide recommendations for a specific plan of action. We note that in this article, the terms women and men refer to cisgender women and cisgender men. The published research cited in this article does not consider pregnancy that occurs in transgender men, non-binary people or intersex people.
This Consensus Statement is the work of an international group of experts, which included clinicians (specializing in neurology, obstetrics and gynaecology, and paediatrics), epidemiologists and basic scientists (specializing in toxicology, endocrinology, reproductive medicine and neurodevelopment). The statement was developed independently of specific societies and colleges by the 13 authors. The process of creating a Consensus Statement was initiated in parallel in Europe (D.M.K., A.M.A., C.-G.B. and B.J.) and the US (Z.L., S.H.S. and A.Z.B.). S.H.S. chaired an initial joint meeting between Z.L., A.Z.B., D.M.K., and after additional consultation with B.J., A.M.A. and C.-G.B., goals and strategy were developed for a joint statement. The expert panel decided not to include respiratory effects, as systematic reviews suggest confounding factors; for example, the presence of respiratory tract infections complicates the evidence15,16,17. D.M.K. and A.Z.B. conducted a comprehensive review of both the experimental and epidemiological literature in English available on PubMed published between 1 January 1995 and 25 October 2020, including systematic reviews, using the following search terms: ‘acetaminophen’ or ‘paracetamol’, ‘endocrine’, ‘reproduction’, ‘urogenital’, ‘neurodevelopment’, ‘attention deficit disorder’, ‘autism spectrum disorder’, ‘hypospadias’, ‘anogenital distance’ and ‘cryptorchidism’. The reference lists of identified papers were then searched for additional relevant articles. Only studies that investigated APAP as an independent exposure were included. All relevant studies are summarized in Supplementary Tables 1–5. After discussion and deliberation amongst the authors, an executive writing group (A.Z.B., S.H.S., B.J. and D.M.K.) wrote the first draft, which was circulated to all authors for critical review. Specific recommendations were accepted after extensive discussion and multiple drafts and revisions by the author group. No one outside the author group was involved in this process. Subsequently, the near final draft was circulated among clinicians, scientists and public health professionals known to the authors in relevant disciplines leading to further comments and revisions. The final statement, which takes into consideration differing international perspectives, prescribing practices and clinical considerations, was supported by 78 signees in addition to the 13 authors (Supplementary Box 1).
APAP use during pregnancy is widespread
APAP is one of the most commonly used medications globally2. In the USA, APAP is estimated to be used by up to 65% of pregnant women18,19. Worldwide, more than 50% of pregnant women are estimated to use APAP18,20,21. APAP has long been considered an option by regulatory bodies such as the FDA and EMA for use in pregnancy for pain and fever when used as directed9,10, as NSAIDs are contraindicated for use in pregnant women in later pregnancy22,23. Pharmacotherapy during pregnancy involves a benefit–risk assessment, in which there is a trade‐off between the potential benefits to the mother and fetus and possible risks to the fetus24. The FDA has formerly given APAP a ‘B’ rating for use in pregnancy in all three trimesters, meaning that animal studies have failed to demonstrate any risks of congenital birth defects from fetal exposure and that no adequate and well-controlled studies have been performed in pregnant women20. In addition, the EMA has found epidemiological data inconclusive and that experimental data do not meet their standards10,25.
During pregnancy, the use of APAP is important for the treatment of high fever and severe pain that, left untreated, could potentially affect the developing fetus or the mother26,27,28,29,30,31. Fever is a well-accepted risk factor for multiple disorders, including neural tube defects and later life cardiovascular disorders32. Most studies, but not all33,34, have suggested that antipyretics such as APAP can reduce this risk32. In a 2020 analysis of daily APAP use in pregnant women, of women classified as APAP users, 8% reported fever as the reason for use35. By contrast, a review of nine cohort studies showed that fever mitigation accounted for APAP use in approximately one-third of women using APAP during pregnancy3. Elective APAP use for the treatment of headache, muscle pain, back pain and infection accounted for APAP use in the majority of women using APAP during pregnancy3,35. Importantly, studies have suggested that in the majority of women using APAP during pregnancy, its use might be without strong indications or have only limited efficacy for such conditions as chronic pain, back and knee pain, as well as headache36,37,38,39,40,41,42. In people who experience migraine headache, including women of reproductive age, studies show that migraine days can be decreased by reducing use of analgesics, including APAP43,44.
Research suggests that women are reluctant to use medications during pregnancy23,45. However, eight out of ten women take at least one prescription or over-the-counter medicine during pregnancy45,46 with APAP being the most common exposure (65%)3,18. Among pregnant women, APAP and antibiotics are believed to have the lowest risk and greatest benefit23. Moreover, APAP usage might be under-reported, as one study showed that when asked about pharmaceutical use, many pregnant women did not report APAP unless specifically asked24.
We call for precautionary action
In this Consensus Statement, we summarize research showing adverse neurological, urogenital and reproductive outcomes associated with maternal and perinatal use of APAP. Based on this experimental and epidemiological literature (Supplementary Tables 1–4), we believe the potential for harm from continued inaction exceeds the harm that might arise from precautionary action. We recognize the limitations of the existing epidemiological literature and the need for rigorous meta-analyses (Supplementary Table 5) and therefore we call for a focused research effort. This effort should include the initiation of epidemiological and experimental studies to understand the hormonal, epigenetic and metabolic mechanisms by which APAP acts and might adversely affect development. Epidemiological studies should be designed specifically with the following goals in mind:
Human epidemiological studies on APAP use in pregnancy should be designed to reduce confounding by indication for use.
Human epidemiological studies on APAP use in pregnancy should be designed to control for genetic factors.
Human epidemiological studies on APAP use in pregnancy should be designed to accurately capture exposure and outcome.
Human epidemiological studies on APAP should be designed to examine timing, dosage and duration of exposure both prenatally and postnatally.
As this combined effort and subsequent systematic reviews will require considerable time and resources, we are proposing precautionary action that can be implemented now.
We recommend that women be counselled prior to or early in pregnancy with the following guidance:
Pregnant women should forego APAP use unless medically indicated.
Pregnant women should consult with their physician or pharmacist if they are uncertain whether use is indicated and before using on a long-term basis.
Pregnant women should minimize risk by using the lowest effective APAP dose for the shortest possible time.
We recommend the following specific actions to implement the goals of raising awareness amongst patients and health-care providers:
The 2015 FDA Drug Safety Communication recommendations should be updated based on evaluation of all available scientific evidence9, including both epidemiological and experimental evidence.
The EMA Pharmacovigilance Risk Assessment Committee should review the most recent research and issue an updated Drug Safety Communication10, including both epidemiological and experimental evidence.
Obstetric and gynaecological associations should review all available research and update their guidance.
The Acetaminophen Awareness Coalition (“Know Your Dose” Campaign) should be expanded to include standardized warnings including that pregnant women should forego APAP use unless medically indicated.
All sales of APAP-containing medications, regardless of country, should be accompanied by recommendations for use in pregnancy. This information should include warning labels on packaging of all APAP-containing medications. If possible, APAP should be sold only from pharmacies (as is currently done in France, Spain, Sweden, Finland and Iceland).
Although these recommendations might not substantially differ from advice currently given to pregnant women, we believe that APAP-specific risk communication between health professionals and pregnant women is warranted due to the high prevalence of use and a widespread perception of negligible risk. APAP use should be minimized but might in some situations, such as high fever and/or severe pain, be the course of action with the lowest risk.
APAP is an endocrine disruptor
Chemicals that disrupt the endocrine system are concerning because they can interfere with the activity of endogenous hormones that are essential for healthy neurological, urogenital and reproductive development2,47,48. APAP is known to readily cross the placenta and blood–brain barrier49,50. During pregnancy, changes occur in APAP metabolism, which might make pregnant women and their fetus more vulnerable to toxic effects. For instance, the molar dose fraction of APAP that is converted to the oxidative metabolite N-acetyl-p-benzoquinone imine might be increased during pregnancy51,52.
The analgesic and antipyretic properties of APAP are still not fully understood. However, several lines of evidence suggest that APAP acts both in the periphery and centrally through several mechanisms. For example, one of the ways APAP is believed to relieve pain is through inhibition of prostaglandin signalling53. Furthermore, APAP inhibits serotonergic mechanisms in clinical studies54. APAP also acts as a prodrug for analgesic metabolites55; in experimental studies, these metabolites activate serotonergic, opioidergic, vanilloid and cannabinoid receptors, as well as transient receptor potential channels53,56. Prostaglandins are lipid compounds with physiologically important roles in the development of the gonads in both sexes and the development of the brain57,58,59; therefore, some of the disrupting effects of APAP are probably mediated through this pathway. Moreover, increasing clinical evidence suggests that the action of APAP in inhibiting prostaglandin signalling in the third trimester can lead to ductus arteriosus constriction, a condition that might result in fetal loss or life-threatening cardiac failure in the newborn60.
In vivo, in vitro and ex vivo studies have shown that APAP directly perturbs hormone-dependent processes, including inhibition of androgen production and increased oestrogen production, disruption of steroidogenesis, depletion of sulfated sex hormones, perturbation of immune function, induction of oxidative stress and indirect activation of the endocannabinoid system1,2,61,62,63,64,65. Independently of APAP, these processes have been implicated as mechanisms related to the development of neurodevelopmental66,67,68,69,70,71,72,73,74,75,76 and reproductive disorders2. In addition to potential effects on neuronal and reproductive development, a combination of clinical studies together with experimental work in animal models and cell lines has also suggested that APAP exposure during pregnancy might decrease fetal haematopoietic stem cell numbers alter steroidogenesis in the placenta and induce placental damage65,77,78,79,80.
Studies of intrauterine APAP exposure have found effects on development in both mouse and rat models. In these studies, doses ranged from the maximum safe dose for a pregnant woman of 50 mg/kg per day to 1,430 mg/kg per day (Supplementary Tables 2, 4)81,82. The majority of studies have used between 200 and 400 mg/kg per day, which is well within the appropriate range for comparing animal and human exposure studies, if the difference in body size is taken into consideration. Hence, for such studies a system of allometry (how anatomy, physiology and behaviour change based on body size) based on body surface area is normally applied, where mouse and rat dose data are divided by a factor of 12.33 and 6.2, respectively, to reach the equivalent human dose83.
Taken together, APAP has many of the key characteristics for hazard identification of an endocrine-disrupting chemical84. However, understanding the exact mechanisms that lead to a particular outcome in humans is complicated as APAP potentially interacts with several critical pathways during development, such as prostaglandins and steroids. Furthermore, the mechanisms leading to APAP-induced reproductive outcomes are probably not the same as those leading to neurological outcomes. In addition, the effect of APAP is dependent on the timing of exposure; for example, any effects on testicular masculinization might not necessarily overlap with the effects on brain masculinization.
Potential urogenital and reproductive effects
Concerns about the safety of APAP in relation to urogenital and reproductive effects have not been addressed in reviews by governmental authorities such as the FDA, or obstetric and gynaecological associations9,85,86. Although some studies have shown no APAP-induced effects, an increasing body of evidence suggests that APAP has the ability to disrupt animal and human reproductive tract development, from fetal life to adulthood in both sexes1,2. Fetal exposure in animal models has been shown experimentally to cause disorders of the male urogenital tract through reduction of androgen action2. Furthermore, experimental models have consistently shown disruption of ovarian development, which results in reduced fertility at the same dose or close to the dose used by pregnant women87,88.
The epidemiological evidence of urogenital and reproductive effects
The relationship between prenatal APAP exposure and urogenital and reproductive abnormalities has been investigated in 11 observational studies in six cohorts including over 130,000 mother–child pairs from different parts of the world24,89,90,91,92,93,94,95,96,97,98 (for a comprehensive review of the literature including effect sizes see Supplementary Table 1). Findings from five of these studies suggest that prenatal APAP exposure is associated with male urogenital and reproductive tract abnormalities, by showing increased risk of male undescended testicles (cryptorchidism)24,89,90 and a reduced anogenital distance (AGD)91,92. An additional study has suggested an association between prenatal APAP exposure and early female puberty93. Four studies have found no increased risk of hypospadias from prenatal APAP exposure94,95,96,97.
AGD is the distance between the anus and the base of the penis, which is an indicator of the degree of masculinization of the genitals51,91,92,99. Both AGD and cryptorchidism are risk factors for reproductive disorders in later life13. Reduced AGD has been found in boys following exposure to APAP during weeks 8–14 of gestation, which coincides with the timing of the masculinization programming window. This period is when male reproductive development (including AGD) is considered to be programmed91,100. Importantly, reduced AGD is recapitulated in mouse and rat experimental studies when animals are exposed in the equivalent rodent programming window (explained later). Another study has demonstrated reduced AGD in boys exposed to the combination of APAP and NSAIDs during pregnancy, suggesting a potential additive effect as exposure to APAP alone did not result in a significant difference in AGD92. Similar additivity with other analgesics has been seen for cryptorchidism, where the association is strongest among mothers using more than one analgesic during pregnancy24. Moreover, exposure to APAP for >2 weeks increased the risk of cryptorchidism24. Most associations for cryptorchidism are seen following long-term APAP exposure (>2 weeks) during late first to early second trimester, which is consistent with the critical time windows for development2,91. Thus, these data suggest that the timing and duration of maternal APAP use are critical factors and that short-term APAP use might be of limited risk.
Although not directly related to evidence of the effects of APAP in utero, studies have also suggested that adult men who used APAP had increased time to pregnancy, decreased testosterone production and had sperm abnormalities, including DNA fragmentation101,102. Moreover, exposure of ex vivo adult testes to APAP has similarly shown a negative effect on testosterone production103. A single cohort study that investigated prenatal APAP exposure and female reproductive outcomes found increasingly earlier attainment of markers of female pubertal development (for example, pubic and axillary hair) with increasing number of weeks of prenatal APAP exposure, in a dose-responsive manner93.
These observational studies controlled for numerous confounding factors but were potentially limited by residual confounding and exposure and outcome misclassification. Confounding by indication for use was controlled for in nine studies24,89,90,93,94,95,97,101,102. Exposure assessment relied on maternal self-reported APAP use in all 11 studies. In these cohorts exposure information was collected in a timely manner to attempt to minimize exposure misclassification and recall bias. Importantly, such misclassification is most likely to be non-differential and result in underestimation of the true effect, rather than to represent spurious associations104.
Together, increasing evidence suggests that prenatal APAP exposure is associated with male urogenital and reproductive tract abnormalities (Fig. 1). Inconsistencies between studies are probably due to differences in assessment methodologies of exposure and outcomes. Moreover, the fact that APAP is a less potent anti-androgen than other pharmaceuticals (for example, ketoconazole) probably means that only large studies would be sufficiently powered to detect effects.
The experimental evidence of urogenital and reproductive effects
Consistent with evidence from epidemiological studies, exposure to APAP has been linked to abnormalities in testicular function, sperm abnormalities and the development of male reproductive disorders across a range of studies involving in vitro, ex vivo and in vivo models (Supplementary Table 2). These data suggest that several mechanisms of action result in decreases in hormones critical for normal reproductive development and inhibition of germ cell proliferation and differentiation. For example, experimental studies have suggested that APAP can reduce testosterone production in the human fetal testis105. Treatment of pregnant mice and rats with APAP has been found to cause urogenital abnormalities, such as reduced AGD in male offspring that is coupled to decreased hormonal levels during the masculinization programming window24,64,105. Differences and inconsistencies remain between studies that might be related to several factors, including species, strain, age, developmental stage, dose, duration, and route and schedule of administration, among others. However, strong evidence from rodent studies and experiments with human cells and tissue performed in several independent laboratories shows that both acute (for example, 24 h) and long-term (for example, 1 week) exposure to APAP results in a reduction in fetal androgens24,105.
Both acute exposure (24 h) and long-term exposure (for example, 1 week ex vivo or from 7 days post coitum to birth in vivo) of rodent and human fetal gonadal tissue to APAP have been demonstrated to adversely affect germ cell development and proliferation81,106. Additionally, prenatal exposure of mice to APAP from 7 days post coitum to birth seems to impair male sexual behaviour in adulthood by disrupting sexual neurobehavioural programming107.
Four independent research teams have found consistently that prenatal APAP exposure can reduce female reproductive health and fertility81,87,88,106,108,109. These teams utilized different models in both rats and mice with APAP exposure at doses equivalent or close to the maximal human recommended dose from 7 days post coitum to birth or from 13.5 days post coitum to birth. The combined data show that APAP exposure results in the reduction of primordial germ cells and delayed meiotic entry, which leads to a decreased number of follicles in adult ovaries and subsequent infertility through early-onset ovarian insufficiency81,106,108,109. Importantly, the effects of APAP on female development have not yet been properly investigated in human observational studies.
Potential neurodevelopmental effects
The developing human brain is uniquely vulnerable to exposure to toxic chemicals. Critical windows of developmental vulnerability occur in utero, and during infancy and early childhood110. During these sensitive life stages, certain chemicals can cause permanent brain injury at low exposure levels111.
The epidemiological evidence of neurodevelopmental effects
The relationships between prenatal APAP exposure and adverse neurodevelopmental outcomes have been investigated in 29 observational studies in 14 cohorts including over 220,000 mother–child pairs from different parts of the world19,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138 (for review of the literature including effect sizes see Supplementary Table 3). Of these studies, 26 identified positive associations with APAP exposure during pregnancy and a range of clinically assessed and parent-reported neurodevelopmental outcomes, primarily attention deficit hyperactivity disorder (ADHD)115,119,120,121,123,126,129,130,131,132,133,134,137,138 and related behavioural abnormalities19,116,117,118,135, but also autism spectrum disorder (ASD)121,124,130, language delays117,118,127,136, decreased IQ113, cerebral palsy122, oppositional–defiant disorder125, decreased executive function112,114 and conduct disorders125. Effect sizes were generally modest but because exposure is widespread1,107, even a small effect size could translate into a large number of affected children. Dose–response has been investigated in 19 studies112,113,114,116,117,118,119,120,121,122,124,127,128,129,130,133,136,137,138 and of these, 16 studies112,114,116,117,118,119,120,121,122,124,127,129,130,133,136,137 identified a dose–response association, whereby increased duration of exposure was associated with increased risk. In many of these studies, associations were weak for short-term exposure suggesting that short-term use might be of limited risk. As with reproductive and urogenital outcomes, exposure timing is important, as the highest risk seemed to occur from exposure during the second and third trimesters of pregnancy (with some exceptions112,113,114). Two studies also investigated APAP exposure during infancy. One study of infant exposure identified associations with decreased mid-childhood executive function and poor behaviour114, whereas the other found no association with cognitive development outcomes19.
These 29 observational studies were limited by potential confounding, including by indication for APAP use, by genetic factors and by bias introduced by exposure and outcome misclassification, as well as study participant loss to follow-up139. Several analytical techniques have been used to control for confounding by indication, with results largely remaining unchanged3,41. Similar disease risk observed across different indications supports a causal association, as different indications (for example, fever and back pain) are unlikely mechanistically to affect disease risk in similar ways140. Using methods such as sibling control design, polygenic risk scores and negative controls, efforts were made to control genetic confounding in 16 studies with little effect on the reported associations in all but two of these studies115,116. APAP exposure assessment relied on maternal self-report in 24 studies, on biomarkers in five studies127,128,129,130,137 and on prescription records in one study138. Although one study that used both biomarkers and self-reported exposure suggested that the two measures of exposure were correlated127, exposure misclassification remains a concern in studies using maternal self-report24. Timely collection of exposure information would probably minimize such exposure misclassification and recall bias. Importantly, misclassification, as mentioned above, is most likely to be non-differential and result in underestimation of the true effect, rather than to represent spurious associations104. The underestimation could be substantial, as evidenced by the far stronger associations reported in biomarker studies127,129,130,137 than in studies relying on self-report.
Two notable studies overcame some of the important limitations of earlier studies. A 2021 study evaluated the association between levels of APAP metabolites in umbilical cord plasma (direct evidence of fetal exposure141) and physician-diagnosed childhood ADHD, ASD and other developmental disabilities, using data from the Boston Birth Cohort130. Cord plasma APAP metabolite concentrations in the first tertile compared with the second and third tertiles were associated with a more than twofold higher odds of an ADHD diagnosis and up to a threefold higher odds of an ASD diagnosis. Sensitivity analyses and subgroup analyses found consistent associations between APAP metabolite concentrations and ADHD and ASD across strata of potential confounders, including maternal indication, substance use, preterm birth, and child age and sex.
In a 2020 prospective cohort study conducted in Québec, Canada, children exposed to APAP prenatally (as measured in meconium) were at increased risk of physician-diagnosed ADHD and hyperactivity, which was indicated by resting-state brain connectivity at ages 6 and 7 years137. Compared with no APAP, detection of APAP in meconium was associated with twice the odds of ADHD. A dose–response association was also detected. Prenatal APAP exposure was also associated with increased negative connectivity between the left prefrontal cortex (frontoparietal seed) and the right precentral gyrus, which mediated the association of APAP with hyperactivity. The authors stated “these results suggest that prior studies may have been biased towards the null by inaccurate maternal recall. Thus, the association between prenatal acetaminophen and ADHD may be even stronger than previously estimated”137. This study established for the first time an association between prenatal APAP exposure and a physical manifestation of neurological alteration. This study not only potentially identifies an underlying mechanism, but also reduces concern that associations found in earlier studies might have been due to diagnostic inaccuracy introduced by suboptimal or subjective outcome measurement139. A limitation of the study is that it did not control for indication; however, when effect sizes are large, as seen in this study, residual confounding by uncontrolled factors is a less likely explanation for identified associations142.
Present biomarker studies are not without limitations in the assessment of exposure. For example, present standard targeted methods are based on analysing free APAP and phase II conjugates after enzymatic deconjugation143. This method captures only part of the metabolic pathway and leaves a fairly short window to assess APAP due to its short half-life (4–6 h)141,143,144, which can lead to underestimation of actual exposure. Thus, a 2021 study suggested that biomarkers identified with standard methods used in biomonitoring are inadequate for human biomonitoring of a non-persistent chemical such as APAP and result in underestimation of actual exposure141.
The experimental evidence of neurodevelopmental effects
Experimental animal studies have suggested that perinatal APAP exposure, even at low therapeutic doses, increases the risk of brain and behavioural abnormalities in rodents51,145,146,147,148,149,150,151, supporting the epidemiological evidence (Supplementary Table 4). A 2019 study suggested that APAP enters the developing rat brain and cerebrospinal fluid in higher amounts than the adult brain. Long-term (5 days) fetal exposure resulted in even higher transfer rates than short-term exposure, which might lead to accumulation of APAP in the fetal brain50. Consistent with the epidemiological data, studies have demonstrated that the strongest effects of long-term use and exposure occur at a time equivalent to the beginning of the third trimester of pregnancy and the time around birth in humans69,148.
APAP effects on the cannabinoid and prostaglandin pathways alone or in combination might be the possible mechanisms1,62,65,69,152,153,154. The antipyretic effect of APAP involves inhibition of prostaglandin-synthesizing cyclooxygenase enzymes in the brain155. Prostaglandin E2 is an endogenous lipid molecule involved in normal brain development, regulating cerebellar development and inducing masculinization of the preoptic area of the brain70. Emerging clinical and molecular research has provided compelling evidence that abnormal cyclooxygenase 2 and prostaglandin E2 signalling is associated with ASD-related pathology and behaviours68,69,154,156,157,158. Other data suggest that the analgesic effect of APAP acts through the endocannabinoid system159. The endocannabinoid system is a complex network of lipid signalling pathways that have an important role in the developing nervous system160. Alterations of the endocannabinoid system have been found in both the brain and the immune system of humans with ASD161,162. Studies in mice have demonstrated the emergence of ASD-like behaviours following diverse genetic or pharmacological manipulations targeting the endocannabinoid system160.
As with reproductive studies, inconsistencies between studies might relate to factors such as species, strain, age, dose, duration of exposure, and route and schedule of administration. However, a particular obstacle is the difficulty in translating human outcomes, such as ADHD and ASD, to behaviour in an animal model. Future studies should include evaluation of brain and behavioural effects in higher order species, from both prenatal and early life exposure, for specific indications and exposure windows153.
This APAP Consensus Statement is a call to prioritize research initiatives and to provide evidence-based medical guidance for APAP use by pregnant women, with the goal of creating awareness so women can make informed decisions that will lead to minimizing APAP exposure. We therefore call for agencies such as the FDA and EMA and appropriate obstetric and gynaecological societies to review all available data covering both epidemiological and experimental studies, so an evidence-based evaluation of the risk can be made available to inform patients and their health-care professionals. The limitations that we identified in the existing literature should be addressed in well-designed research that accurately captures medication use during pregnancy and minimizes potential confounding by indication and exposure misclassification.
We here recognize our professional and social responsibility to take this action, even in the face of uncertainty, in light of the serious consequences of inaction. This call to action is consistent with the 2016 Targeting Environmental Neuro-Developmental Risks (TENDR) Consensus Statement47, which we support:
“We as a society should be able to take protective action when scientific evidence indicates a chemical is of concern, and not wait for unequivocal proof that a chemical is causing harm to our children. Evidence of neurodevelopmental toxicity of any type — epidemiological or toxicological or mechanistic — by itself should constitute a signal sufficient to trigger prioritization and some level of action.”47.
In addition, a new opinion statement issued by the American College of Obstetricians and Gynecologists suggests that gynaecologists should screen patients for exposure to environmental chemicals before and during pregnancy and counsel on how to minimize risks. We support this statement, which is consistent with our recommendations163.
APAP is a modifiable exposure. We recognize that limited medical alternatives exist to treat pain and fever; however, we believe the combined weight of animal and human scientific evidence is strong enough for pregnant women to be cautioned by health professionals against its indiscriminate use, both as a single ingredient and in combination with other medications. We recommend that APAP should be used by pregnant women cautiously at the lowest effective dose for the shortest possible time. Long-term or high-dose use should be limited to indications as advised by a health professional. Packaging should include warning labels including these recommendations. Given the high prevalence of APAP use by pregnant women, the public health implications of use reduction might be substantial.
Konkel, L. Reproductive headache? Investigating acetaminophen as a potential endocrine disruptor. Environ. Health Perspect. 126, 032001 (2018).
Kristensen, D. M. et al. Analgesic use – prevalence, biomonitoring and endocrine and reproductive effects. Nat. Rev. Endocrinol. 12, 381–393 (2016).
Bauer, A. Z., Kriebel, D., Herbert, M. R., Bornehag, C.-G. & Swan, S. H. Prenatal paracetamol exposure and child neurodevelopment: a review. Horm. Behav. 101, 125–147 (2018).
Markets and Research. Global Acetaminophen Market 2020 by Manufacturers, Regions, Type and Application, Forecast to 2026. Marketsandresearch.biz https://www.marketsandresearch.biz/report/43101/global-acetaminophen-market-2020-by-manufacturers-regions-type-and-application-forecast-to-2026 (2020).
Larson, A. M. et al. Acetaminophen-induced acute liver failure: results of a United States multicenter, prospective study. Hepatology 42, 1364–1372 (2005).
Rotundo, L. & Pyrsopoulos, N. Liver injury induced by paracetamol and challenges associated with intentional and unintentional use. World J. Hepatol. 12, 125–136 (2020).
Berardi, G., Tuckfield, L., DelVecchio, M. T. & Aronoff, S. Differential diagnosis of acute liver failure in children: a systematic review. Pediatr. Gastroenterol. Hepatol. Nutr. 23, 501–510 (2020).
Li, J., Chiew, A. L., Isbister, G. K. & Duffull, S. B. Sulfate conjugation may be the key to hepatotoxicity in paracetamol overdose. Br. J. Clin. Pharmacol. 87, 2392–2396 (2021).
Food and Drug Administration. FDA Drug Safety Communications: FDA has reviewed possible risks of pain medicine use during pregnancy. https://www.fda.gov/media/90209/download (2015).
European Medicines Agency. PRAC recommendations on signals: adopted at the 12–15 March 2019 PRAC meeting. https://www.ema.europa.eu/en/documents/prac-recommendation/prac-recommendations-signals-adopted-12-15-march-2019-prac-meeting_en.pdf (2019).
Zablotsky, B. et al. Prevalence and trends of developmental disabilities among children in the US: 2009–2017. Pediatrics 144, e20190811 (2019).
De Jonge, C. & Barratt, C. L. R. The present crisis in male reproductive health: an urgent need for a political, social, and research roadmap. Andrology 7, 762–768 (2019).
Skakkebaek, N. E. et al. Male reproductive disorders and fertility trends: influences of environment and genetic susceptibility. Physiol. Rev. 96, 55–97 (2016).
Levine, H. et al. Temporal trends in sperm count: a systematic review and meta-regression analysis. Hum. Reprod. Update 23, 646–659 (2017).
Weatherall, M., Ioannides, S., Braithwaite, I. & Beasley, R. The association between paracetamol use and asthma: causation or coincidence? Clin. Exp. Allergy 45, 108–113 (2015).
Fan, G., Wang, B., Liu, C. & Li, D. Prenatal paracetamol use and asthma in childhood: a systematic review and meta-analysis. Allergol. Immunopathol. 45, 528–533 (2017).
Cheelo, M. et al. Paracetamol exposure in pregnancy and early childhood and development of childhood asthma: a systematic review and meta-analysis. Arch. Dis. Child. 100, 81–89 (2015).
Werler, M. M., Mitchell, A. A., Hernandez-Diaz, S. & Honein, M. A. Use of over-the-counter medications during pregnancy. Am. J. Obstet. Gynecol. 193, 771–777 (2005).
Bertoldi, A. D. et al. Associations of acetaminophen use during pregnancy and the first year of life with neurodevelopment in early childhood. Paediatr. Perinat. Epidemiol. 34, 267–277 (2020).
Servey, J. & Chang, J. Over-the-counter medications in pregnancy. Am. Fam. Physician 90, 548–555 (2014).
Masarwa, R. et al. Prenatal exposure to acetaminophen and risk for attention deficit hyperactivity disorder and autistic spectrum disorder: a systematic review, meta-analysis, and meta-regression analysis of cohort studies. Am. J. Epidemiol. 187, 1817–1827 (2018).
Li, D.-K., Ferber, J. R., Odouli, R. & Quesenberry, C. Use of nonsteroidal antiinflammatory drugs during pregnancy and the risk of miscarriage. Am. J. Obstet. Gynecol. 219, 275.e1–275.e8 (2018).
Ceulemans, M. et al. Women’s beliefs about medicines and adherence to pharmacotherapy in pregnancy: opportunities for community pharmacists. Curr. Pharm. Des. 25, 469–482 (2019).
Kristensen, D. M. et al. Intrauterine exposure to mild analgesics is a risk factor for development of male reproductive disorders in human and rat. Hum. Reprod. 26, 235–244 (2011).
Black, E. et al. Medication use and pain management in pregnancy: a critical review. Pain. Pract. 19, 875–899 (2019).
Croen, L. A. et al. Infection and fever in pregnancy and autism spectrum disorders: findings from the study to explore early development. Autism Res. 12, 1551–1561 (2019).
Gustavson, K. et al. Maternal fever during pregnancy and offspring attention deficit hyperactivity disorder. Sci. Rep. 9, 9519 (2019).
Brucato, M. et al. Prenatal exposure to fever is associated with autism spectrum disorder in the Boston Birth Cohort. Autism Res. 10, 1878–1890 (2017).
Källén, B. & Reis, M. Ongoing pharmacological management of chronic pain in pregnancy. Drugs 76, 915–924 (2016).
Dreier, J. W., Andersen, A.-M. N. & Berg-Beckhoff, G. Systematic review and meta-analyses: fever in pregnancy and health impacts in the offspring. Pediatrics 133, e674–e688 (2014).
Sass, L. et al. Fever in pregnancy and the risk of congenital malformations: a cohort study. BMC Pregnancy Childbirth 17, 413 (2017).
Graham, J. M. J. Update on the gestational effects of maternal hyperthermia. Birth Defects Res. 112, 943–952 (2020).
Li, Z. et al. Maternal flu or fever, medication use, and neural tube defects: a population-based case-control study in Northern China. Birth. Defects Res. A. Clin. Mol. Teratol. 79, 295–300 (2007).
Wang, M., Wang, Z.-P., Gong, R. & Zhao, Z.-T. Maternal flu or fever, medications use in the first trimester and the risk for neural tube defects: a hospital-based case-control study in China. Childs Nerv. Syst. 30, 665–671 (2014).
Bandoli, G., Palmsten, K. & Chambers, C. Acetaminophen use in pregnancy: examining prevalence, timing, and indication of use in a prospective birth cohort. Paediatr. Perinat. Epidemiol. 34, 237–246 (2020).
Saragiotto, B. T. et al. Paracetamol for low back pain. Cochrane Database Syst. Rev. 2016, CD012230 (2016).
Jefferies, S. et al. Randomized controlled trial of the effect of regular paracetamol on influenza infection. Respirology 21, 370–377 (2016).
Ennis, Z. N., Dideriksen, D., Vaegter, H. B., Handberg, G. & Pottegård, A. Acetaminophen for chronic pain: a systematic review on efficacy. Basic Clin. Pharmacol. Toxicol. 118, 184–189 (2016).
Nazarko, L. Does paracetamol help or hinder healing in bacterial infections? Br. J. Community Nurs. 19, 335–339 (2014).
Leopoldino, A. O. et al. Paracetamol versus placebo for knee and hip osteoarthritis. Cochrane Database Syst. Rev. 2, CD013273 (2019).
Olsen, J. & Liew, Z. Fetal programming of mental health by acetaminophen? Response to the SMFM statement: prenatal acetaminophen use and ADHD. Expert Opin. Drug Saf. 16, 1395–1398 (2017).
Stephens, G., Derry, S. & Moore, R. A. Paracetamol (acetaminophen) for acute treatment of episodic tension-type headache in adults. Cochrane Database Syst. Rev. 2016, CD011889 (2016).
Engelstoft, I. M. S. et al. Complete withdrawal is the most feasible treatment for medication-overuse headache: a randomized controlled open-label trial. Eur. J. Pain. 23, 1162–1170 (2019).
Tassorelli, C. et al. A consensus protocol for the management of medication-overuse headache: evaluation in a multicentric, multinational study. Cephalalgia Int. J. Headache 34, 645–655 (2014).
Nordeng, H., Ystrøm, E. & Einarson, A. Perception of risk regarding the use of medications and other exposures during pregnancy. Eur. J. Clin. Pharmacol. 66, 207–214 (2010).
Lupattelli, A. et al. Medication use in pregnancy: a cross-sectional, multinational web-based study. BMJ Open 4, e004365 (2014).
Bennett, D. et al. Project TENDR: targeting environmental neuro-developmental risks the TENDR consensus statement. Environ. Health Perspect. 124, A118–A122 (2016).
Wilson, H. A., Creighton, C., Scharfman, H., Choleris, E. & MacLusky, N. J. Endocrine insights into the pathophysiology of autism spectrum disorder. Neuroscientist https://doi.org/10.1177/1073858420952046 (2020).
Levy, G., Garrettson, L. K. & Soda, D. M. Letter: evidence of placental transfer of acetaminophen. Pediatrics 55, 895 (1975).
Koehn, L., Habgood, M., Huang, Y., Dziegielewska, K. & Saunders, N. Determinants of drug entry into the developing brain. F1000Research 8, 1372 (2019).
Zafeiri, A., Mitchell, R. T., Hay, D. C. & Fowler, P. A. Over-the-counter analgesics during pregnancy: a comprehensive review of global prevalence and offspring safety. Hum. Reprod. Update 27, 67–95 (2021).
Mian, P. et al. Physiologically based pharmacokinetic modeling to characterize acetaminophen pharmacokinetics and N-acetyl-p-benzoquinone imine (NAPQI) formation in non-pregnant and pregnant women. Clin. Pharmacokinet. 59, 97–110 (2020).
Graham, G. G., Davies, M. J., Day, R. O., Mohamudally, A. & Scott, K. F. The modern pharmacology of paracetamol: therapeutic actions, mechanism of action, metabolism, toxicity and recent pharmacological findings. Inflammopharmacology 21, 201–232 (2013).
Pickering, G., Estève, V., Loriot, M.-A., Eschalier, A. & Dubray, C. Acetaminophen reinforces descending inhibitory pain pathways. Clin. Pharmacol. Ther. 84, 47–51 (2008).
Högestätt, E. D. et al. Conversion of acetaminophen to the bioactive N-acylphenolamine AM404 via fatty acid amide hydrolase-dependent arachidonic acid conjugation in the nervous system. J. Biol. Chem. 280, 31405–31412 (2005).
Andersson, D. A. et al. TRPA1 mediates spinal antinociception induced by acetaminophen and the cannabinoid Δ(9)-tetrahydrocannabiorcol. Nat. Commun. 2, 551 (2011).
Amateau, S. K. & McCarthy, M. M. Induction of PGE2 by estradiol mediates developmental masculinization of sex behavior. Nat. Neurosci. 7, 643–650 (2004).
Adams, I. R. & McLaren, A. Sexually dimorphic development of mouse primordial germ cells: switching from oogenesis to spermatogenesis. Development 129, 1155–1164 (2002).
Lim, H. et al. Multiple female reproductive failures in cyclooxygenase 2-deficient mice. Cell 91, 197–208 (1997).
Allegaert, K., Mian, P., Lapillonne, A. & van den Anker, J. N. Maternal paracetamol intake and fetal ductus arteriosus constriction or closure: a case series analysis. Br. J. Clin. Pharmacol. 85, 245–251 (2019).
Cohen, I. V. et al. Acetaminophen (paracetamol) use modifies the sulfation of sex hormones. EBioMedicine 28, 316–323 (2018).
Gould, G. G. et al. Acetaminophen differentially enhances social behavior and cortical cannabinoid levels in inbred mice. Prog. Neuropsychopharmacol. Biol. Psychiatry 38, 260–269 (2012).
Klopcic, I., Markovic, T., Mlinaric-Rascan, I. & Sollner Dolenc, M. Endocrine disrupting activities and immunomodulatory effects in lymphoblastoid cell lines of diclofenac, 4-hydroxydiclofenac and paracetamol. Toxicol. Lett. 294, 95–104 (2018).
Holm, J. B. et al. Aniline is rapidly converted into paracetamol impairing male reproductive development. Toxicol. Sci. 148, 288–298 (2015).
Addo, K. A., Palakodety, N. & Fry, R. C. Acetaminophen modulates the expression of steroidogenesis-associated genes and estradiol levels in human placental JEG-3 cells. Toxicol. Sci. 179, 44–52 (2021).
Arambula, S. E. & McCarthy, M. M. Neuroendocrine-immune crosstalk shapes sex-specific brain development. Endocrinology 161, bqaa055 (2020).
Reilly, J., Gallagher, L., Leader, G. & Shen, S. Coupling of autism genes to tissue-wide expression and dysfunction of synapse, calcium signalling and transcriptional regulation. PLoS ONE 15, e0242773 (2020).
Rai-Bhogal, R. et al. Maternal exposure to prostaglandin E(2) modifies expression of Wnt genes in mouse brain – an autism connection. Biochem. Biophys. Rep. 14, 43–53 (2018).
Dean, S. L., Knutson, J. F., Krebs-Kraft, D. L. & McCarthy, M. M. Prostaglandin E2 is an endogenous modulator of cerebellar development and complex behavior during a sensitive postnatal period. Eur. J. Neurosci. 35, 1218–1229 (2012).
McCarthy, M. M. & Wright, C. L. Convergence of sex differences and the neuroimmune system in autism spectrum disorder. Biol. Psychiatry 81, 402–410 (2017).
Tsai, C.-S. et al. Phthalates, para-hydroxybenzoic acids, bisphenol-A, and gonadal hormones’ effects on susceptibility to attention-deficit/hyperactivity disorder. Toxics 8, 57 (2020).
Müller, D. et al. The neuroendocrine modulation of global DNA methylation in neuropsychiatric disorders. Mol. Psychiatry 26, 66–69 (2021).
Pietropaolo, S., Bellocchio, L., Bouzón-Arnáiz, I. & Yee, B. K. The role of the endocannabinoid system in autism spectrum disorders: evidence from mouse studies. Prog. Mol. Biol. Transl. Sci. 173, 183–208 (2020).
Needham, B. D. et al. Plasma and fecal metabolite profiles in autism spectrum disorder. Biol. Psychiatry 89, 451–462 (2021).
Baron-Cohen, S. et al. Foetal oestrogens and autism. Mol. Psychiatry 25, 2970–2978 (2020).
Allegaert, K. A critical review on the relevance of paracetamol for procedural pain management in neonates. Front. Pediatr. 8, 89 (2020).
Thiele, K. et al. Prenatal acetaminophen affects maternal immune and endocrine adaptation to pregnancy, induces placental damage, and impairs fetal development in mice. Am. J. Pathol. 185, 2805–2818 (2015).
Karimi, K. et al. Prenatal acetaminophen induces liver toxicity in dams, reduces fetal liver stem cells, and increases airway inflammation in adult offspring. J. Hepatol. 62, 1085–1091 (2015).
Burman, A. et al. Acetaminophen attenuates invasion and alters the expression of extracellular matrix enzymes and vascular factors in human first trimester trophoblast cells. Placenta 104, 146–160 (2020).
Bremer, L. et al. Paracetamol medication during pregnancy: insights on intake frequencies, dosages and effects on hematopoietic stem cell populations in cord blood from a longitudinal prospective pregnancy cohort. EBioMedicine 26, 146–151 (2017).
Holm, J. B. et al. Intrauterine exposure to paracetamol and aniline impairs female reproductive development by reducing follicle reserves and fertility. Toxicol. Sci. 150, 178–189 (2016).
Reel, J. R., Lawton, A. D. & Lamb, J. C. Reproductive toxicity evaluation of acetaminophen in Swiss CD-1 mice using a continuous breeding protocol. Fundam. Appl. Toxicol. 18, 233–239 (1992).
Reagan-Shaw, S., Nihal, M. & Ahmad, N. Dose translation from animal to human studies revisited. FASEB J. 22, 659–661 (2008).
La Merrill, M. A. et al. Consensus on the key characteristics of endocrine-disrupting chemicals as a basis for hazard identification. Nat. Rev. Endocrinol. 16, 45–57 (2020).
Bisson, D., Newell, S. & Laxton, C. on behalf of the Royal College of Obstetricians and Gynaecologists. Antenatal and postnatal analgesia: Scientific Impact Paper No. 59. BJOG 126, e114–e124 (2019).
Society for Maternal-Fetal Medicine Publications Committee. Prenatal acetaminophen use and outcomes in children. Am. J. Obstet. Gynecol. 216, B14–B15 (2017).
Arendrup, F. S., Mazaud-Guittot, S., Jegou, B. & Kristensen, D. M. EDC IMPACT: is exposure during pregnancy to acetaminophen/paracetamol disrupting female reproductive development? Endocr. Connect. 7, 149–158 (2018).
Rossitto, M. et al. In utero exposure to acetaminophen and ibuprofen leads to intergenerational accelerated reproductive aging in female mice. Commun. Biol. 2, 310 (2019).
Jensen, M. S. et al. Maternal use of acetaminophen, ibuprofen, and acetylsalicylic acid during pregnancy and risk of cryptorchidism. Epidemiology 21, 779–785 (2010).
Snijder, C. A. et al. Intrauterine exposure to mild analgesics during pregnancy and the occurrence of cryptorchidism and hypospadia in the offspring: the Generation R Study. Hum. Reprod. 27, 1191–1201 (2012).
Fisher, B. G. et al. Prenatal paracetamol exposure is associated with shorter anogenital distance in male infants. Hum. Reprod. 31, 2642–2650 (2016).
Lind, D. V. et al. Maternal use of mild analgesics during pregnancy associated with reduced anogenital distance in sons: a cohort study of 1027 mother-child pairs. Hum. Reprod. 32, 223–231 (2017).
Ernst, A. et al. Acetaminophen (paracetamol) exposure during pregnancy and pubertal development in boys and girls from a nationwide puberty cohort. Am. J. Epidemiol. 188, 34–46 (2019).
Interrante, J. D. et al. Risk comparison for prenatal use of analgesics and selected birth defects, National Birth Defects Prevention Study 1997–2011. Ann. Epidemiol. 27, 645–653.e2 (2017).
Feldkamp, M. L., Meyer, R. E., Krikov, S. & Botto, L. D. Acetaminophen use in pregnancy and risk of birth defects: findings from the National Birth Defects Prevention Study. Obstet. Gynecol. 115, 109–115 (2010).
Lind, J. N. et al. Maternal medication and herbal use and risk for hypospadias: data from the National Birth Defects Prevention Study, 1997–2007. Pharmacoepidemiol. Drug Saf. 22, 783–793 (2013).
Rebordosa, C. et al. Acetaminophen use during pregnancy: effects on risk for congenital abnormalities. Am. J. Obstet. Gynecol. 198, 178.e1–178.e7 (2008).
Wagner-Mahler, K. et al. Prospective study on the prevalence and associated risk factors of cryptorchidism in 6246 newborn boys from Nice area, France. Int. J. Androl. 34, e499–e510 (2011).
Schwartz, C. L. et al. Anogenital distance as a toxicological or clinical marker for fetal androgen action and risk for reproductive disorders. Arch. Toxicol. 93, 253–272 (2019).
Welsh, M. et al. Identification in rats of a programming window for reproductive tract masculinization, disruption of which leads to hypospadias and cryptorchidism. J. Clin. Invest. 118, 1479–1490 (2008).
Smarr, M. M., Kannan, K., Chen, Z., Kim, S. & Buck Louis, G. M. Male urinary paracetamol and semen quality. Andrology 5, 1082–1088 (2017).
Smarr, M. M. et al. Urinary paracetamol and time-to-pregnancy. Hum. Reprod. 31, 2119–2127 (2016).
Albert, O. et al. Paracetamol, aspirin and indomethacin display endocrine disrupting properties in the adult human testis in vitro. Hum. Reprod. 28, 1890–1898 (2013).
Pearce, N., Checkoway, H. & Kriebel, D. Bias in occupational epidemiology studies. Occup. Environ. Med. 64, 562–568 (2007).
van den Driesche, S. et al. Prolonged exposure to acetaminophen reduces testosterone production by the human fetal testis in a xenograft model. Sci. Transl. Med. 7, 288ra80 (2015).
Hurtado-Gonzalez, P. et al. Effects of exposure to acetaminophen and ibuprofen on fetal germ cell development in both sexes in rodent and human using multiple experimental systems. Environ. Health Perspect. 126, 047006 (2018).
Hay-Schmidt, A. et al. Paracetamol/acetaminophen impairs brain masculinisation. Reproduction 154, 145–152 (2017).
Dean, A. et al. Analgesic exposure in pregnant rats affects fetal germ cell development with inter-generational reproductive consequences. Sci. Rep. 6, 19789 (2016).
Johansson, H. K. L. et al. Perinatal exposure to mixtures of endocrine disrupting chemicals reduces female rat follicle reserves and accelerates reproductive aging. Reprod. Toxicol. 61, 186–194 (2016).
Rice, D. & Barone, S. J. Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Environ. Health Perspect. 108 (Suppl 3), 511–533 (2000).
Grandjean, P. & Landrigan, P. J. Neurobehavioural effects of developmental toxicity. Lancet Neurol. 13, 330–338 (2014).
Liew, Z., Bach, C. C., Asarnow, R. F., Ritz, B. & Olsen, J. Paracetamol use during pregnancy and attention and executive function in offspring at age 5 years. Int. J. Epidemiol. 45, 2009–2017 (2016).
Liew, Z., Ritz, B., Virk, J., Arah, O. A. & Olsen, J. Prenatal use of acetaminophen and child IQ: a Danish cohort study. Epidemiology 27, 912–918 (2016).
Rifas-Shiman, S. L. et al. Associations of prenatal or infant exposure to acetaminophen or ibuprofen with mid-childhood executive function and behaviour. Paediatr. Perinat. Epidemiol. 34, 287–298 (2020).
Leppert, B. et al. Association of maternal neurodevelopmental risk alleles with early-life exposures. JAMA Psychiatry 76, 834–842 (2019).
Tronnes, J. N., Wood, M., Lupattelli, A., Ystrom, E. & Nordeng, H. Prenatal paracetamol exposure and neurodevelopmental outcomes in preschool-aged children. Paediatr. Perinat. Epidemiol. 34, 247–256 (2020).
Brandlistuen, R. E., Ystrom, E., Nulman, I., Koren, G. & Nordeng, H. Prenatal paracetamol exposure and child neurodevelopment: a sibling-controlled cohort study. Int. J. Epidemiol. 42, 1702–1713 (2013).
Vlenterie, R. et al. Neurodevelopmental problems at 18 months among children exposed to paracetamol in utero: a propensity score matched cohort study. Int. J. Epidemiol. 45, 1998–2008 (2016).
Ystrom, E. et al. Prenatal exposure to acetaminophen and risk of ADHD. Pediatrics 140, e20163840 (2017).
Liew, Z., Ritz, B., Rebordosa, C., Lee, P. C. & Olsen, J. Acetaminophen use during pregnancy, behavioral problems, and hyperkinetic disorders. JAMA Pediatr. 168, 313–320 (2014).
Liew, Z., Ritz, B., Virk, J. & Olsen, J. Maternal use of acetaminophen during pregnancy and risk of autism spectrum disorders in childhood: a Danish national birth cohort study. Autism Res. 9, 951–958 (2016).
Petersen, T. G. et al. Use of paracetamol, ibuprofen or aspirin in pregnancy and risk of cerebral palsy in the child. Int. J. Epidemiol. 47, 121–130 (2018).
Thompson, J. M. D., Waldie, K. E., Wall, C. R., Murphy, R. & Mitchell, E. A. Associations between acetaminophen use during pregnancy and ADHD symptoms measured at ages 7 and 11 years. PLoS ONE 9, e108210 (2014).
Avella-Garcia, C. B. et al. Acetaminophen use in pregnancy and neurodevelopment: attention function and autism spectrum symptoms. Int. J. Epidemiol. 45, 1987–1996 (2016).
Ruisch, I. H., Buitelaar, J. K., Glennon, J. C., Hoekstra, P. J. & Dietrich, A. Pregnancy risk factors in relation to oppositional-defiant and conduct disorder symptoms in the Avon Longitudinal Study of Parents and Children. J. Psychiatr. Res. 101, 63–71 (2018).
Stergiakouli, E., Thapar, A. & Davey Smith, G. Association of acetaminophen use during pregnancy with behavioral problems in childhood: evidence against confounding. JAMA Pediatr. 170, 964–970 (2016).
Bornehag, C. G. et al. Prenatal exposure to acetaminophen and children’s language development at 30 months. Eur. Psychiatry 51, 98–103 (2018).
Laue, H. E. et al. Association between meconium acetaminophen and childhood neurocognitive development in GESTE, a Canadian cohort study. Toxicol. Sci. 167, 138–144 (2019).
Ji, Y. et al. Maternal biomarkers of acetaminophen use and offspring attention deficit hyperactivity disorder. Brain Sci. 8, 127 (2018).
Ji, Y. et al. Association of cord plasma biomarkers of in utero acetaminophen exposure with risk of attention-deficit/hyperactivity disorder and autism spectrum disorder in childhood. JAMA Psychiatry 77, 180–189 (2020).
Tovo-Rodrigues, L. et al. Is intrauterine exposure to acetaminophen associated with emotional and hyperactivity problems during childhood? Findings from the 2004 Pelotas birth cohort. BMC Psychiatry 18, 368 (2018).
Liew, Z. et al. Use of negative control exposure analysis to evaluate confounding: an example of acetaminophen exposure and attention-deficit/hyperactivity disorder in Nurses’ Health Study II. Am. J. Epidemiol. 188, 768–775 (2019).
Gervin, K., Nordeng, H., Ystrom, E., Reichborn-Kjennerud, T. & Lyle, R. Long-term prenatal exposure to paracetamol is associated with DNA methylation differences in children diagnosed with ADHD. Clin. Epigenetics 9, 77 (2017).
Golding, J. et al. Associations between paracetamol (acetaminophen) intake between 18 and 32 weeks gestation and neurocognitive outcomes in the child: a longitudinal cohort study. Paediatr. Perinat. Epidemiol. 34, 257–266 (2020).
Tovo-Rodrigues, L. et al. Low neurodevelopmental performance and behavioural/emotional problems at 24 and 48 months in Brazilian children exposed to acetaminophen during foetal development. Paediatr. Perinat. Epidemiol. 34, 278–286 (2020).
Skovlund, E., Handal, M., Selmer, R., Brandlistuen, R. E. & Skurtveit, S. Language competence and communication skills in 3-year-old children after prenatal exposure to analgesic opioids. Pharmacoepidemiol. Drug Saf. 26, 625–634 (2017).
Baker, B. H. et al. Association of prenatal acetaminophen exposure measured in meconium with risk of attention-deficit/hyperactivity disorder mediated by frontoparietal network brain connectivity. JAMA Pediatr. 174, 1073–1081 (2020).
Chen, M.-H. et al. Prenatal exposure to acetaminophen and the risk of attention-deficit/hyperactivity disorder: a nationwide study in Taiwan. J. Clin. Psychiatry 80, 18m12612 (2019).
Wood, M. E. Associations between prenatal acetaminophen exposure and child neurodevelopment: truth, bias, or a bit of both? Paediatr. Perinat. Epidemiol. 34, 233–236 (2020).
Liew, Z. & Ernst, A. Intrauterine exposure to acetaminophen and adverse developmental outcomes: epidemiological findings and methodological issues. Curr. Environ. Health Rep. 8, 23–33 (2021).
David, A. et al. Acetaminophen metabolism revisited using non-targeted analyses: implications for human biomonitoring. Env. Int. 149, 106388 (2021).
Aschengrau, A. & Seage, G. in Essentials of Epidemiology in Public Health. 3rd edn, p373 (Jones and Bartlett, 2014).
Modick, H., Weiss, T., Dierkes, G., Brüning, T. & Koch, H. M. Ubiquitous presence of paracetamol in human urine: sources and implications. Reproduction 147, R105–R117 (2014).
Prescott, L. F. Kinetics and metabolism of paracetamol and phenacetin. Br. J. Clin. Pharmacol. 10 (Suppl 2), 291S–298S (1980).
Blecharz-Klin, K. et al. Early paracetamol exposure decreases brain-derived neurotrophic factor (BDNF) in striatum and affects social behaviour and exploration in rats. Pharmacol. Biochem. Behav. 168, 25–32 (2018).
Blecharz-Klin, K. et al. Paracetamol – effect of early exposure on neurotransmission, spatial memory and motor performance in rats. Behav. Brain Res. 323, 162–171 (2017).
Viberg, H., Eriksson, P., Gordh, T. & Fredriksson, A. Paracetamol (acetaminophen) administration during neonatal brain development affects cognitive function and alters its analgesic and anxiolytic response in adult male mice. Toxicol. Sci. 138, 139–147 (2014).
Philippot, G., Gordh, T., Fredriksson, A. & Viberg, H. Adult neurobehavioral alterations in male and female mice following developmental exposure to paracetamol (acetaminophen): characterization of a critical period. J. Appl. Toxicol. 37, 1174–1181 (2017).
Hay-Schmidt, A. et al. Prenatal exposure to paracetamol/acetaminophen and precursor aniline impairs masculinisation of male brain and behaviour. Reproduction 154, 145–152 (2017).
Klein, R. M. et al. Gestational exposure to paracetamol in rats induces neurofunctional alterations in the progeny. Neurotoxicol. Teratol. 77, 106838 (2020).
Rigobello, C. et al. Perinatal exposure to paracetamol: dose and sex-dependent effects in behaviour and brain’s oxidative stress markers in progeny. Behav. Brain Res. 408, 113294 (2021).
de Fays, L. et al. Use of paracetamol during pregnancy and child neurological development. Dev. Med. Child. Neurol. 57, 718–724 (2015).
Allegaert, K. & van den Anker, J. How to translate neuro-cognitive and behavioural outcome data in animals exposed to paracetamol to the human perinatal setting? Arch. Med. Sci. https://doi.org/10.5114/aoms.2020.100715 (2020).
Wright, C. L., Hoffman, J. H. & McCarthy, M. M. Evidence that inflammation promotes estradiol synthesis in human cerebellum during early childhood. Transl. Psychiatry 9, 58 (2019).
Mirrasekhian, E. et al. The antipyretic effect of paracetamol occurs independent of transient receptor potential ankyrin 1-mediated hypothermia and is associated with prostaglandin inhibition in the brain. FASEB J. 32, 5751–5759 (2018).
Wong, C. T., Bestard-Lorigados, I. & Crawford, D. A. Autism-related behaviors in the cyclooxygenase-2-deficient mouse model. Genes. Brain Behav. 18, e12506 (2019).
Addo, K. A. et al. Acetaminophen use during pregnancy and DNA methylation in the placenta of the extremely low gestational age newborn (ELGAN) cohort. Environ. Epigenetics 5, dvz010 (2019).
Hoffman, J. F., Wright, C. L. & McCarthy, M. M. A critical period in Purkinje cell development is mediated by local estradiol synthesis, disrupted by inflammation, and has enduring consequences only for males. J. Neurosci. 36, 10039–10049 (2016).
Przybyła, G. W., Szychowski, K. A. & Gmiński, J. Paracetamol – an old drug with new mechanisms of action. Clin. Exp. Pharmacol. Physiol. https://doi.org/10.1111/1440-1681.13392 (2020).
Fyke, W., Alarcon, J. M., Velinov, M. & Chadman, K. K. Pharmacological inhibition of the primary endocannabinoid producing enzyme, DGL-α, induces autism spectrum disorder-like and co-morbid phenotypes in adult C57BL/J mice. Autism Res. 14, 1375–1389 (2021).
Schultz, S., Gould, G. G., Antonucci, N., Brigida, A. L. & Siniscalco, D. Endocannabinoid system dysregulation from acetaminophen use may lead to autism spectrum disorder: could cannabinoid treatment be efficacious? Molecules 26, 1845 (2021).
Brigida, A. L., Schultz, S., Cascone, M., Antonucci, N. & Siniscalco, D. Endocannabinod signal dysregulation in autism spectrum disorders: a correlation link between inflammatory state and neuro-immune alterations. Int. J. Mol. Sci. 18, 1425 (2017).
American College of Obstetricians and Gynecologists. Reducing prenatal exposure to toxic environmental agents. Committee Opinion Number 832. https://www.acog.org/en/clinical/clinical-guidance/committee-opinion/articles/2021/07/reducing-prenatal-exposure-to-toxic-environmental-agents (2021).
R.T.M. acknowledges the support of a UKRI Future Leaders Fellowship (MR/S017151/1).
R.T. Mitchell is supported by a UKRI Future Leaders Fellowship (MR/S017151/1). All the other authors declare no competing interests.
We dedicate this article to the memory of Bernard Jégou, who died prematurely after its acceptance. We are profoundly indebted to Bernard, not only for his work on this manuscript, but most importantly for his significant personal contribution to the recent advances in the field of endocrine disruption that are described here and for his friendship and generosity.
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Consumer Health Products Association — acetaminophen: https://www.chpa.org/our-issues/otc-medicines/acetaminophen
The Acetaminophen Awareness Coalition “Know your dose” campaign: https://www.knowyourdose.org/the-acetaminophen-awareness-coalition/
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Bauer, A.Z., Swan, S.H., Kriebel, D. et al. Paracetamol use during pregnancy — a call for precautionary action. Nat Rev Endocrinol 17, 757–766 (2021). https://doi.org/10.1038/s41574-021-00553-7
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