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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 LERCANIDIPINE Cause Product use issue? 14 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Product use issue have been filed in association with LERCANIDIPINE. This represents 0.4% of all adverse event reports for LERCANIDIPINE.

14
Reports of Product use issue with LERCANIDIPINE
0.4%
of all LERCANIDIPINE reports
0
Deaths
9
Hospitalizations

How Dangerous Is Product use issue From LERCANIDIPINE?

Of the 14 reports, 9 (64.3%) required hospitalization, and 1 (7.1%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for LERCANIDIPINE. However, 14 reports have been filed with the FAERS database.

What Other Side Effects Does LERCANIDIPINE Cause?

Acute kidney injury (424) Hypotension (401) Fall (323) Hypertension (197) Hyperkalaemia (176) Drug ineffective (149) Diarrhoea (122) Hyponatraemia (122) Renal impairment (120) Oedema peripheral (114)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which LERCANIDIPINE Alternatives Have Lower Product use issue Risk?

LERCANIDIPINE vs LETAIRIS LERCANIDIPINE vs LETERMOVIR LERCANIDIPINE vs LETROZOLE LERCANIDIPINE vs LETROZOLE\RIBOCICLIB LERCANIDIPINE vs LEUCOVORIN

Related Pages

LERCANIDIPINE Full Profile All Product use issue Reports All Drugs Causing Product use issue LERCANIDIPINE Demographics