Does LAMOTRIGINE Cause Suspected product quality issue? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Suspected product quality issue have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 0.0% of all adverse event reports for LAMOTRIGINE.
9
Reports of Suspected product quality issue with LAMOTRIGINE
0.0%
of all LAMOTRIGINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Suspected product quality issue From LAMOTRIGINE?
Of the 9 reports, 2 (22.2%) required hospitalization.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 9 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 Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which LAMOTRIGINE Alternatives Have Lower Suspected product quality issue Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM