Does LOSARTAN Cause Product dose omission? 38 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 38 reports of Product dose omission have been filed in association with LOSARTAN (Losartan Potassium). This represents 0.2% of all adverse event reports for LOSARTAN.
38
Reports of Product dose omission with LOSARTAN
0.2%
of all LOSARTAN reports
2
Deaths
12
Hospitalizations
How Dangerous Is Product dose omission From LOSARTAN?
Of the 38 reports, 2 (5.3%) resulted in death, 12 (31.6%) required hospitalization, and 2 (5.3%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOSARTAN. However, 38 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?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which LOSARTAN Alternatives Have Lower Product dose omission Risk?
LOSARTAN vs LOSARTAN\LOSARTAN
LOSARTAN vs LOTEPREDNOL ETABONATE
LOSARTAN vs LOTEPREDNOL ETABONATE\TOBRAMYCIN
LOSARTAN vs LOTILANER
LOSARTAN vs LOVASTATIN