Does LAMOTRIGINE Cause Wrong patient received product? 112 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 112 reports of Wrong patient received product have been filed in association with LAMOTRIGINE (Lamotrigine ER). This represents 0.2% of all adverse event reports for LAMOTRIGINE.
112
Reports of Wrong patient received product with LAMOTRIGINE
0.2%
of all LAMOTRIGINE reports
25
Deaths
50
Hospitalizations
How Dangerous Is Wrong patient received product From LAMOTRIGINE?
Of the 112 reports, 25 (22.3%) resulted in death, 50 (44.6%) required hospitalization, and 31 (27.7%) were considered life-threatening.
Is Wrong patient received product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LAMOTRIGINE. However, 112 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 Wrong patient received product?
INSULIN LISPRO (334)
CLOZAPINE (198)
RISPERIDONE (176)
OXAZEPAM (152)
BISOPROLOL (150)
LEVETIRACETAM (126)
ACETAMINOPHEN (123)
METFORMIN (116)
INSULIN GLARGINE (114)
CLONAZEPAM (112)
Which LAMOTRIGINE Alternatives Have Lower Wrong patient received product Risk?
LAMOTRIGINE vs LANADELUMAB
LAMOTRIGINE vs LANADELUMAB-FLYO
LAMOTRIGINE vs LANREOTIDE
LAMOTRIGINE vs LANSOPRAZOLE
LAMOTRIGINE vs LANTHANUM