Does LAMOTRIGINE Cause Intentional product use issue? 669 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 669 reports of Intentional product use issue have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 1.4% of all adverse event reports for LAMOTRIGINE.
669
Reports of Intentional product use issue with LAMOTRIGINE
1.4%
of all LAMOTRIGINE reports
560
Deaths
512
Hospitalizations
How Dangerous Is Intentional product use issue From LAMOTRIGINE?
Of the 669 reports, 560 (83.7%) resulted in death, 512 (76.5%) required hospitalization, and 489 (73.1%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 669 reports have been filed with the FAERS database.
What Other Side Effects Does LAMOTRIGINE Cause?
Drug ineffective (5,175)
Seizure (3,459)
Toxicity to various agents (3,256)
Rash (3,249)
Foetal exposure during pregnancy (2,985)
Off label use (2,625)
Completed suicide (2,433)
Drug reaction with eosinophilia and systemic symptoms (2,235)
Dizziness (2,170)
Pyrexia (1,967)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which LAMOTRIGINE Alternatives Have Lower Intentional product use issue Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM