Does FELODIPINE Cause Incorrect product administration duration? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Incorrect product administration duration have been filed in association with FELODIPINE (Felodipine). This represents 1.4% of all adverse event reports for FELODIPINE.
21
Reports of Incorrect product administration duration with FELODIPINE
1.4%
of all FELODIPINE reports
0
Deaths
21
Hospitalizations
How Dangerous Is Incorrect product administration duration From FELODIPINE?
Of the 21 reports, 21 (100.0%) required hospitalization, and 1 (4.8%) 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 FELODIPINE. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does FELODIPINE Cause?
Fatigue (519)
Headache (499)
Palpitations (495)
Abdominal discomfort (490)
Pyrexia (487)
Tinnitus (480)
Pain (479)
Covid-19 (477)
Migraine (472)
Off label use (441)
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 FELODIPINE Alternatives Have Lower Incorrect product administration duration Risk?
FELODIPINE vs FENFLURAMINE
FELODIPINE vs FENOFIBRATE
FELODIPINE vs FENOFIBRIC ACID
FELODIPINE vs FENOTEROL
FELODIPINE vs FENOTEROL HYDROBROMIDE