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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does LACOSAMIDE Cause Wrong patient received product? 40 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 40 reports of Wrong patient received product have been filed in association with LACOSAMIDE (Lacosamide). This represents 0.2% of all adverse event reports for LACOSAMIDE.

40
Reports of Wrong patient received product with LACOSAMIDE
0.2%
of all LACOSAMIDE reports
16
Deaths
22
Hospitalizations

How Dangerous Is Wrong patient received product From LACOSAMIDE?

Of the 40 reports, 16 (40.0%) resulted in death, 22 (55.0%) required hospitalization.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LACOSAMIDE. However, 40 reports have been filed with the FAERS database.

What Other Side Effects Does LACOSAMIDE Cause?

Seizure (4,585) Drug ineffective (2,945) Off label use (2,811) Dizziness (974) Overdose (971) Generalised tonic-clonic seizure (918) Epilepsy (902) Status epilepticus (874) Fall (780) Somnolence (768)

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 LACOSAMIDE Alternatives Have Lower Wrong patient received product Risk?

LACOSAMIDE vs LACTOBACILLUS ACIDOPHILUS LACOSAMIDE vs LACTOBACILLUS RHAMNOSUS LACOSAMIDE vs LACTOSE LACOSAMIDE vs LACTULOSE LACOSAMIDE vs LAMICTAL

Related Pages

LACOSAMIDE Full Profile All Wrong patient received product Reports All Drugs Causing Wrong patient received product LACOSAMIDE Demographics