Perinatal EvidenceCompass
Prepopulated workbenchMED-065

Mood stabilizers/antiseizure — other

Gabapentin

Antiseizure medication with off-label psychiatric use; established bipolar efficacy must not be assumed

Not a categorical safety rating

This record organizes questions; it does not close them.

The clinical fields and position statements are prepopulated from the public-source corpus. They have not completed individual dual extraction, formal appraisal, exact-label reconciliation, or multidisciplinary sign-off. Do not use this page to justify abrupt discontinuation or reflexive switching.

Inventory identity

What this record represents

Canonical generic name
Gabapentin
Entity type
single-ingredient drug
Active component(s)
Gabapentin
Formulation / route / interval
Oral; formulation varies
Attachment entry
Gabapentin
Separate monograph status
No — cross-reference shared molecule monograph
Identity and cross-reference
Also: anxiety, insomnia, and alcohol/cannabis use-disorder research
Inventory verification confidence
Moderate — molecule-level source; exact product/jurisdiction pending

Decision taxonomy

Five positions kept separate

These are workbench statements for reviewer execution. They are not independently commissioned, patient-specific recommendations.

  1. 01

    Stable continuation

    Workbench statement

    Do not withhold or discontinue solely because of pregnancy or lactation. For this record, assess indication, prior response, relapse severity, dose/formulation, alternatives, exposure timing, and mapped evidence; individual commissioned adjudication remains pending.

  2. 02

    New initiation in pregnancy

    Workbench statement

    For a new start, prefer an effective option with the strongest diagnosis-specific efficacy and reproductive evidence when clinically suitable. This record has not received an individual, independently verified initiation ranking.

  3. 03

    Switch before conception

    Workbench statement

    Before conception, consider a switch only when expected benefit exceeds relapse, withdrawal, failed-switch, and dual-exposure risks. Build and monitor the plan before pregnancy when feasible; no universal switch direction is assigned here.

  4. 04

    Unplanned exposure

    Workbench statement

    After unplanned exposure, confirm product, route, dose, timing, indication, co-exposures, and symptoms; do not advise abrupt cessation. Use the mapped evidence and current label to decide whether any targeted fetal assessment is indicated.

  5. 05

    Delivery, postpartum & lactation

    Workbench statement

    Create separate delivery, postpartum-dose, neonatal-observation, and lactation plans. Do not infer breastfeeding suitability from pregnancy evidence or routinely taper before delivery without drug-specific support.

Linked evidence

3 mapped claim summaries

Mapping can include class-wide, framework, formulation, regulatory, or evidence-gap claims. A linked claim is not necessarily a drug-specific causal estimate.

B-020Provisional public source

Early gabapentin exposure was not associated with a clear overall major-malformation increase, but a cardiac signal could not be excluded.

Public-source certainty descriptor
moderate—large claims cohort
Formal appraisal
Not started — full text and independent appraisal pending
Exposure window
first trimester
Comparator
unexposed pregnancies
Effect or numbers carried forward

No clear overall MCM association after adjustment; imprecise cardiac concern

Limitations

Prescription fills, residual confounding by pain/epilepsy/opioids, and outcome misclassification.

Sources, citation controls, and verification state

Linked sources

PMID
Not populated in v0.95
DOI
Pending DOI verification
Exact locator
Pending exact table/figure/page/supplement locator
Access date
2026-07-29
Integrity check
Same-day source surveillance recorded; source-by-source correction/retraction verification remains pending
Internal verification
Source-linked; independent external verification pending
B-021Provisional public source

Late or sustained gabapentin exposure was associated with preterm birth, SGA, and NICU admission.

Public-source certainty descriptor
low-to-moderate—observational claims cohort
Formal appraisal
Not started — full text and independent appraisal pending
Exposure window
late pregnancy or exposure throughout pregnancy
Comparator
unexposed pregnancies
Effect or numbers carried forward

Directionally increased PTB, SGA, and NICU outcomes in adjusted analyses

Limitations

Strong potential for confounding by indication, opioid use, smoking, and illness severity.

Sources, citation controls, and verification state

Linked sources

PMID
Not populated in v0.95
DOI
Pending DOI verification
Exact locator
Pending exact table/figure/page/supplement locator
Access date
2026-07-29
Integrity check
Same-day source surveillance recorded; source-by-source correction/retraction verification remains pending
Internal verification
Source-linked; independent external verification pending
B-031Provisional public source

Once pregnancy is established, replacing an effective antiseizure medicine requires caution because seizure recurrence can harm the pregnant patient and fetus.

Public-source certainty descriptor
guideline recommendation
Formal appraisal
Not started — full text and independent appraisal pending
Exposure window
after conception
Comparator
continuing effective therapy
Effect or numbers carried forward

No single effect estimate; AAN/AES/SMFM caution

Limitations

Decision varies by seizure syndrome, prior control, dose, and drug-specific fetal risk.

Sources, citation controls, and verification state
PMID
Not populated in v0.95
DOI
Pending DOI verification
Exact locator
Pending exact table/figure/page/supplement locator
Access date
2026-07-29
Integrity check
Same-day source surveillance recorded; source-by-source correction/retraction verification remains pending
Internal verification
Source-linked; independent external verification pending