Does LOSARTAN Cause Recalled product? 23 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Recalled product have been filed in association with LOSARTAN (Losartan Potassium). This represents 0.1% of all adverse event reports for LOSARTAN.
23
Reports of Recalled product with LOSARTAN
0.1%
of all LOSARTAN reports
2
Deaths
5
Hospitalizations
How Dangerous Is Recalled product From LOSARTAN?
Of the 23 reports, 2 (8.7%) resulted in death, 5 (21.7%) required hospitalization, and 5 (21.7%) were considered life-threatening.
Is Recalled product Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOSARTAN. However, 23 reports have been filed with the FAERS database.
What Other Side Effects Does LOSARTAN Cause?
Drug ineffective (1,640)
Dizziness (1,553)
Headache (1,256)
Dyspnoea (1,185)
Malaise (1,149)
Hypotension (1,139)
Fatigue (1,116)
Acute kidney injury (1,100)
Cough (1,073)
Blood pressure increased (950)
What Other Drugs Cause Recalled product?
PARATHYROID HORMONE (900)
ANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT (80)
CALCITRIOL (68)
CALCIUM (66)
REMDESIVIR (36)
LEVOTHYROXINE\LIOTHYRONINE (34)
TESTOSTERONE (32)
VALSARTAN (32)
CHLORHEXIDINE (28)
ALCOHOL (26)
Which LOSARTAN Alternatives Have Lower Recalled product Risk?
LOSARTAN vs LOSARTAN\LOSARTAN
LOSARTAN vs LOTEPREDNOL ETABONATE
LOSARTAN vs LOTEPREDNOL ETABONATE\TOBRAMYCIN
LOSARTAN vs LOTILANER
LOSARTAN vs LOVASTATIN