Does LOSARTAN Cause Product dose omission in error? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product dose omission in error have been filed in association with LOSARTAN (Losartan Potassium). This represents 0.1% of all adverse event reports for LOSARTAN.
17
Reports of Product dose omission in error with LOSARTAN
0.1%
of all LOSARTAN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission in error From LOSARTAN?
Of the 17 reports, 3 (17.6%) required hospitalization, and 1 (5.9%) were considered life-threatening.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOSARTAN. However, 17 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 Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which LOSARTAN Alternatives Have Lower Product dose omission in error Risk?
LOSARTAN vs LOSARTAN\LOSARTAN
LOSARTAN vs LOTEPREDNOL ETABONATE
LOSARTAN vs LOTEPREDNOL ETABONATE\TOBRAMYCIN
LOSARTAN vs LOTILANER
LOSARTAN vs LOVASTATIN