Does CANDESARTAN Cause Incorrect product administration duration? 83 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 83 reports of Incorrect product administration duration have been filed in association with CANDESARTAN. This represents 0.9% of all adverse event reports for CANDESARTAN.
83
Reports of Incorrect product administration duration with CANDESARTAN
0.9%
of all CANDESARTAN reports
63
Deaths
75
Hospitalizations
How Dangerous Is Incorrect product administration duration From CANDESARTAN?
Of the 83 reports, 63 (75.9%) resulted in death, 75 (90.4%) required hospitalization, and 63 (75.9%) 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 CANDESARTAN. However, 83 reports have been filed with the FAERS database.
What Other Side Effects Does CANDESARTAN Cause?
Off label use (1,911)
Fatigue (1,468)
Dyspnoea (1,456)
Pain (1,455)
Drug ineffective (1,428)
Headache (1,371)
Nausea (1,282)
Dizziness (1,237)
Vomiting (1,202)
Diarrhoea (1,145)
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 CANDESARTAN Alternatives Have Lower Incorrect product administration duration Risk?
CANDESARTAN vs CANDESARTAN CILEXETIL
CANDESARTAN vs CANDESARTAN CILEXETIL\HYDROCHLOROTHIAZIDE
CANDESARTAN vs CANGRELOR
CANDESARTAN vs CANIS LUPUS FAMILIARIS SKIN
CANDESARTAN vs CANNABIDIOL