Amphetamine
MedicationAdderall, Dexedrine, Dexedrine Spansules, Dextrostat, Liquadd, ProCentra, Zenzedi
Prescription stimulant
Research strength: 3 / 5
MotherToBaby reports that studies of prescribed mixed amphetamine salts and dextroamphetamine have not found a higher chance of birth defects, and a large first-trimester cohort of 5,571 amphetamine exposures found no increase in overall or heart malformations. MotherToBaby says miscarriage findings are mixed; the current U.S. Adderall XR label says available research has not identified a drug-associated risk of major birth defects or miscarriage, while also stating that it may cause fetal harm and noting premature delivery and low birth weight. A 2025 Norwegian study linked ADHD medicines as a group to miscarriage; its reported drug-specific increases were for methylphenidate, lisdexamfetamine, and atomoxetine, not amphetamine. FDA's boxed warning says Adderall XR has a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction; misuse and abuse can result in overdose and death. Ask your provider about your situation.
Last reviewed: 2026-10-16
Sources
- MotherToBaby: Dextroamphetamine-Amphetamine (Adderall)Teratology service
- Huybrechts et al., JAMA Psychiatry 2018 (International Pregnancy Safety Study)US government
- DailyMed: ADDERALL XR prescribing information (Takeda, revised April 2026)Drug company label
- Srinivas et al., British Journal of Psychiatry 2025 (Norwegian miscarriage study)US government
- FDA: Prescription stimulant boxed-warning update, May 11, 2023US government
Research strength: 3 / 5
MotherToBaby reports mixed findings on poor growth, low birth weight, early delivery, high blood pressure, and preeclampsia with prescribed amphetamines, and says ADHD or other factors may also affect those outcomes. In a large U.S. Medicaid cohort, first-half amphetamine/dextroamphetamine use was associated with higher preeclampsia risk after adjustment, while most other placental outcomes did not show clear increases. The U.S. label says amphetamines may lower blood flow to the placenta and notes early delivery and low birth weight; available studies do not give a separate estimate for the second trimester alone. Recent Norway-Sweden and Australian cohorts found some higher preterm, blood-pressure, or diabetes outcomes with ADHD medicines overall, but these results were not specific to amphetamine and may reflect ADHD or other factors. FDA's boxed warning says Adderall XR has a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction; misuse and abuse can result in overdose and death. Ask your provider about your situation.
Last reviewed: 2026-10-16
Sources
- MotherToBaby: Dextroamphetamine-Amphetamine (Adderall)Teratology service
- Cohen et al., Obstetrics & Gynecology 2017 (Medicaid cohort)US government
- Srinivas et al., Paediatric and Perinatal Epidemiology 2026 (Norway-Sweden preterm cohort)US government
- Sit et al., Archives of Women's Mental Health 2026 (NSW cohort)US government
- DailyMed: ADDERALL XR prescribing information (Takeda, revised April 2026)Drug company label
- FDA: Prescription stimulant boxed-warning update, May 11, 2023US government
Research strength: 3 / 5
MotherToBaby reports mixed findings on early delivery and high blood pressure or preeclampsia in studies of prescribed amphetamines, and says the condition being treated may also affect these outcomes. A large U.S. study found that continuing stimulant treatment after 20 weeks was associated with preterm birth compared with stopping, but that comparison combined amphetamine/dextroamphetamine and methylphenidate. A Norway-Sweden study found duration-related preterm-birth signals for ADHD medicines during weeks 22 to 36, and a U.S. cohort found similar directions in amphetamine- and methylphenidate-stratified analyses; neither provides a separate third-trimester estimate or settles amphetamine-specific risk. The current U.S. label notes increased risks of premature delivery and low birth weight and tells clinicians to monitor exposed newborns for feeding problems, irritability, agitation, or excessive drowsiness. FDA's boxed warning says Adderall XR has a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction; misuse and abuse can result in overdose and death. Ask your provider about your situation.
Last reviewed: 2026-10-16
Sources
- MotherToBaby: Dextroamphetamine-Amphetamine (Adderall)Teratology service
- Cohen et al., Obstetrics & Gynecology 2017 (Medicaid cohort)US government
- Srinivas et al., Paediatric and Perinatal Epidemiology 2026 (Norway-Sweden preterm cohort)US government
- Hasan et al., Journal of Attention Disorders 2026 (U.S. claims cohort)US government
- DailyMed: ADDERALL XR prescribing information (Takeda, revised April 2026)Drug company label
- FDA: Prescription stimulant boxed-warning update, May 11, 2023US government
Amphetamine — Breastfeeding
Research strength: 2 / 5
MotherToBaby reports that there are no studies of the mixed amphetamine-dextroamphetamine combination during breastfeeding, while small studies of dextroamphetamine or amphetamine found no problems in infant health, growth, or development. The 2024 pilot followed 13 children exposed to amphetamine stimulants during breastfeeding; its abstract reported normal neurodevelopment and no significant adverse effects. LactMed's account of that study lists nonspecific symptoms in five children, though overall development was reported normal, and long-term effects remain unknown. LactMed says some experts allow therapeutic doses with infant monitoring, while the current Adderall XR label says breastfeeding is not recommended during treatment. FDA's boxed warning says Adderall XR has a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction; misuse and abuse can result in overdose and death. Ask your provider about your situation.
Last reviewed: 2026-10-16
Sources
- MotherToBaby: Dextroamphetamine-Amphetamine (Adderall)Teratology service
- MotherToBaby: DextroamphetamineTeratology service
- Benassayag Kaduri et al., Psychiatry Research 2024 (breastfeeding pilot)US government
- LactMed (NIH): AmphetamineUS government
- DailyMed: ADDERALL XR prescribing information (Takeda, revised April 2026)Drug company label
- FDA: Prescription stimulant boxed-warning update, May 11, 2023US government
Pregnancy
Birth defects: Huybrechts et al. (2018) studied 1,813,894 U.S. Medicaid pregnancies and 2,560,069 Nordic live-birth pregnancies. The U.S. first-trimester analysis included 5,571 amphetamine-exposed pregnancies and found adjusted relative risks of 1.05 (95% CI, 0.93-1.19) for any major malformation and 0.96 (0.78-1.19) for cardiac malformations. Both cohorts included live births only, so they could miss affected pregnancies that ended earlier. Placental outcomes: Cohen et al. (2017) found first-half amphetamine/dextroamphetamine exposure associated with preeclampsia after adjustment (RR 1.33, 95% CI 1.12-1.58), while most other early-pregnancy outcomes were not clearly increased. Continuing stimulant monotherapy after 20 weeks was associated with preterm birth compared with stopping (RR 1.30, 95% CI 1.10-1.55), but this estimate combined amphetamine/dextroamphetamine and methylphenidate. Russell et al. (2024) compared 547 dexamphetamine continuers, 297 who ceased during pregnancy, and 844 unexposed women; ceasers had higher odds of threatened abortion than continuers. The study could not examine pregnancy losses before 20 weeks and cautioned that sample size and timing limited interpretation. Child development: Suarez et al. (2024) studied two U.S. claims cohorts and found adjusted amphetamine/dextroamphetamine exposure was not meaningfully associated with autism, ADHD, or a combined neurodevelopmental outcome. Bang Madsen et al. (2025) found no statistically clear increase in Swedish medication-type analyses, but the amphetamine group estimates were imprecise. Recent studies add class-level evidence: a 2025 Norwegian miscarriage study reported increased odds for ADHD medication overall, with specific reported increases for methylphenidate, lisdexamfetamine, and atomoxetine, not an amphetamine-specific estimate. A Norway-Sweden cohort of 11,075 pregnancies found higher preterm risk with at least two early fills and with longer late-pregnancy exposure to ADHD medicines; it did not establish an amphetamine-specific effect. A 2026 U.S. claims cohort, an Australian cardiometabolic cohort, and an August 2026 U.S. electronic-record cohort reported some class-level associations with continued or in-pregnancy medication use, but causal effects and amphetamine-specific risks remain uncertain. A 2025 systematic review of 12 cohorts found mixed results and recommended individualized discussion; it did not pool a single risk estimate.
Breastfeeding
MotherToBaby reports no direct study of the mixed amphetamine-dextroamphetamine combination during breastfeeding. LactMed summarizes small milk-level reports and says that some evidence suggests prescribed amphetamine does not adversely affect nursing infants, but long-term neurological development has not been well studied. The 2024 pilot followed 13 children exposed to amphetamine stimulants through breastfeeding and its abstract reported normal neurodevelopment with no significant adverse effects; the small sample cannot rule out uncommon or longer-term effects. LactMed's detailed account of that study reports nonspecific adverse effects in five children, including somnolence, crying or restlessness, and colic or constipation, while reporting normal development overall. LactMed notes that large doses might interfere with milk production, especially before supply is established, and says some experts allow therapeutic doses with infant monitoring. MotherToBaby also says product labels note that large doses could lower milk supply, but that clear reports of this effect have not been described. The current Adderall XR label says breastfeeding is not recommended during treatment because of the potential for serious adverse reactions, while also noting that long-term neurodevelopmental effects are unknown.
Amphetamine is a prescription central nervous system stimulant. Adderall contains mixed amphetamine salts, while dextroamphetamine is a related amphetamine medicine. Lisdexamfetamine is converted in the body to dextroamphetamine, so its studies may be relevant to some questions but are not direct evidence for mixed amphetamine salts.
What was tested
Pregnancy evidence mainly comes from prescription and dispensing records linked to birth and health records, not randomized trials. The largest malformation study focused on first-trimester exposure and live births; other cohorts studied placental outcomes, continuation or stopping, and child development. Several 2025-2026 studies analyze ADHD medicines as a class and do not isolate amphetamine. Prescription fills do not prove a medicine was taken, and observational studies may retain confounding from ADHD severity, smoking, other health conditions, or other medicines. Breastfeeding evidence consists mainly of case reports, milk measurements, and one small 13-child pilot; long-term infant effects remain uncertain.
Pregnancy product-label advice and clinical treatment planning
- Source A says
- The UK Amfexa product information says dexamfetamine use during pregnancy is not recommended and says women planning pregnancy should discontinue it. (Amfexa 10 mg Tablets Summary of Product Characteristics (UK eMC))
- Source B says
- U.S. Adderall XR labeling says published epidemiologic and postmarketing data have not identified a drug-associated risk of major birth defects or miscarriage. Scoten et al. recommend individualized planning and considering pharmacotherapy for moderate or severe ADHD after weighing treatment and untreated-condition risks. (DailyMed: ADDERALL XR prescribing information (Takeda), Scoten et al., American Journal of Obstetrics and Gynecology 2024 (perinatal ADHD guideline))
- Why they differ
- The UK product information takes a more restrictive position, while the U.S. label reports no identified risk for major birth defects or miscarriage but also describes possible premature delivery and low birth weight. The clinical review weighs medication exposure against the effects of inadequately treated ADHD. These are different label and clinical-review approaches to observational evidence, not proof that either approach applies to every patient.
- Other sources
- MotherToBaby describes mixed findings for placental outcomes, and primary cohorts report no increased malformation risk overall but an adjusted preeclampsia signal for amphetamine/dextroamphetamine. (MotherToBaby: Dextroamphetamine-Amphetamine (Adderall), Huybrechts et al., JAMA Psychiatry 2018 (International Pregnancy Safety Study), Cohen et al., Obstetrics & Gynecology 2017 (Medicaid cohort))
- What the evidence shows overall
- Keep the rating at guidance. The evidence does not support a universal avoid recommendation, but the preeclampsia finding, possible later pregnancy outcomes, and differing product-label advice warrant an individualized discussion.
Breastfeeding recommendations
- Source A says
- The current U.S. Adderall XR label says breastfeeding is not recommended during treatment because of the potential for serious adverse reactions in nursing infants. (DailyMed: ADDERALL XR prescribing information (Takeda))
- Source B says
- LactMed says some experts allow therapeutic amphetamine doses during nursing with infant monitoring. The 2024 pilot abstract reported normal neurodevelopment and no significant adverse effects among 13 exposed children, though LactMed lists nonspecific symptoms in five children. (LactMed (NIH): Amphetamine, Benassayag Kaduri et al., Psychiatry Research 2024 (breastfeeding pilot))
- Why they differ
- The label takes a precautionary position, while LactMed and the small human study weigh limited prescribed-use observations. LactMed's account of the pilot reports nonspecific symptoms in some children, although the abstract reports no significant adverse effects and normal neurodevelopment. Long-term infant effects are not well studied, and the pilot is too small to rule out uncommon effects.
- What the evidence shows overall
- Keep guidance and state both positions. The pilot does not overturn the product-label warning or establish that all doses and situations have the same effects.
Breastfeeding pilot outcomes as described in the abstract and LactMed
- Source A says
- The 2024 pilot abstract reports normal neurodevelopment with no significant adverse effects among 13 children exposed to amphetamine stimulants through breastfeeding. (Benassayag Kaduri et al., Psychiatry Research 2024 (breastfeeding pilot))
- Source B says
- LactMed's detailed summary of the same cohort lists nonspecific adverse effects in five children: somnolence in one, crying or restlessness in three, and colic or constipation in four. It also reports normal gross motor development and neurodevelopment scores overall. (LactMed (NIH): Amphetamine)
- Why they differ
- The abstract gives the study's overall conclusion, while LactMed reports symptom-level details. The reports are not necessarily incompatible because the listed symptoms were nonspecific and the study reported normal developmental scores, but the abstract alone could leave the impression that no symptoms occurred.
- What the evidence shows overall
- Describe the small pilot as having normal overall developmental results while noting the nonspecific symptoms reported in LactMed. Do not treat 13 children as enough to establish uncommon or long-term effects.
Newborn withdrawal after prescribed pregnancy use
- Source A says
- MotherToBaby reports that withdrawal has not been reported in newborns when mothers took mixed amphetamine salts or dextroamphetamine as prescribed. (MotherToBaby: Dextroamphetamine-Amphetamine (Adderall))
- Source B says
- The current U.S. product label tells clinicians to monitor infants born to mothers taking amphetamines for withdrawal symptoms, including feeding difficulty, irritability, agitation, and excessive drowsiness. (DailyMed: ADDERALL XR prescribing information (Takeda))
- Why they differ
- MotherToBaby describes the available reports after prescribed use, while the label gives a broader monitoring instruction. The absence of published reports does not establish that symptoms cannot occur.
- What the evidence shows overall
- Describe both statements and keep the label's monitoring language. Available sources do not establish how often withdrawal symptoms occur after prescribed treatment.
- Scoten et al. describe individualized treatment planning and say pharmacotherapy can be considered for moderate or severe ADHD while weighing medication risks against the risks of inadequately treated ADHD. (Scoten et al., AJOG 2024)
- MotherToBaby says to discuss medication changes with healthcare providers because stopping suddenly can cause withdrawal; it notes that a provider may discuss gradual dose reduction. (MotherToBaby: Dextroamphetamine-Amphetamine (Adderall))
General research, not specific to pregnancy.
FDA's 2023 class update requires boxed-warning information about abuse, misuse, addiction, and overdose for prescription stimulants. FDA's 2025 extended-release update focuses on children younger than 6, who had higher drug exposure and more adverse effects, including weight loss, than older children at the same dose.
- The FDA boxed warning says Adderall XR has a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction; misuse and abuse can result in overdose and death. (FDA: Prescription stimulant boxed-warning update, May 11, 2023, DailyMed: ADDERALL XR prescribing information (Takeda))
- FDA revised extended-release stimulant labeling to warn that patients younger than 6 may have higher drug exposure and higher rates of side effects, including weight loss, than older children taking the same dose. (FDA: Expanded labeling for weight-loss risk in patients younger than 6 taking extended-release stimulants, June 30, 2025)
- MotherToBaby: Dextroamphetamine-Amphetamine (Adderall)Teratology serviceSecondary
- MotherToBaby: DextroamphetamineTeratology serviceSecondary
- LactMed (NIH): AmphetamineUS governmentSecondaryPage dated 2025-06-15
- DailyMed: ADDERALL XR prescribing information (Takeda)Drug company labelTertiary
- FDA: Prescription stimulant boxed-warning update, May 11, 2023US governmentSecondaryPage dated 2023-05-11
- FDA: Expanded labeling for weight-loss risk in patients younger than 6 taking extended-release stimulants, June 30, 2025US governmentSecondaryPage dated 2025-06-30
- Amfexa 10 mg Tablets Summary of Product Characteristics (UK eMC)TertiaryPage dated 2026-05-05
- Huybrechts et al., JAMA Psychiatry 2018 (International Pregnancy Safety Study)US governmentPrimaryIndependent check
- Cohen et al., Obstetrics & Gynecology 2017 (Medicaid cohort)US governmentPrimaryIndependent check
- Russell et al., Archives of Women's Mental Health 2024 (Western Australia cohort)US governmentPrimaryIndependent check
- Suarez et al., JAMA Psychiatry 2024 (U.S. linked cohort)US governmentPrimaryIndependent check
- Bang Madsen et al., Molecular Psychiatry 2025 (Swedish cohort and meta-analysis)US governmentPrimaryIndependent check
- Srinivas et al., British Journal of Psychiatry 2025 (Norwegian miscarriage study)US governmentPrimaryIndependent check
- Srinivas et al., Paediatric and Perinatal Epidemiology 2026 (Norway-Sweden preterm cohort)US governmentPrimaryIndependent check
- Hasan et al., Journal of Attention Disorders 2026 (U.S. claims cohort)US governmentPrimaryIndependent check
- Sit et al., Archives of Women's Mental Health 2026 (New South Wales cohort)US governmentPrimaryIndependent check
- Benassayag Kaduri et al., Psychiatry Research 2024 (breastfeeding pilot)US governmentPrimaryIndependent check
- Scoten et al., American Journal of Obstetrics and Gynecology 2024 (perinatal ADHD guideline)US governmentSecondaryIndependent check
- Maternal and offspring outcomes associated with prescribed ADHD medication in pregnancy: a systematic review, 2025US governmentPrimaryIndependent check
- Obstetric Risk Associated With Stimulant Versus Nonstimulant Treatment During Pregnancy, 2026US governmentPrimaryIndependent check
Last reviewed 2026-10-16
Independent check 2026-10-16
Not yet clinician-reviewed
Ask your provider about your situation.
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