Does LAMOTRIGINE Cause Product quality issue? 601 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 601 reports of Product quality issue have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 1.3% of all adverse event reports for LAMOTRIGINE.
601
Reports of Product quality issue with LAMOTRIGINE
1.3%
of all LAMOTRIGINE reports
425
Deaths
362
Hospitalizations
How Dangerous Is Product quality issue From LAMOTRIGINE?
Of the 601 reports, 425 (70.7%) resulted in death, 362 (60.2%) required hospitalization, and 359 (59.7%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 601 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 Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which LAMOTRIGINE Alternatives Have Lower Product quality issue Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM