Does LAMOTRIGINE Cause Incorrect product administration duration? 68 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 68 reports of Incorrect product administration duration have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 0.1% of all adverse event reports for LAMOTRIGINE.
68
Reports of Incorrect product administration duration with LAMOTRIGINE
0.1%
of all LAMOTRIGINE reports
63
Deaths
64
Hospitalizations
How Dangerous Is Incorrect product administration duration From LAMOTRIGINE?
Of the 68 reports, 63 (92.6%) resulted in death, 64 (94.1%) required hospitalization, and 62 (91.2%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 68 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which LAMOTRIGINE Alternatives Have Lower Incorrect product administration duration Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM