Does LOSARTAN Cause Intentional product use issue? 67 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 67 reports of Intentional product use issue have been filed in association with LOSARTAN (Losartan Potassium). This represents 0.3% of all adverse event reports for LOSARTAN.
67
Reports of Intentional product use issue with LOSARTAN
0.3%
of all LOSARTAN reports
1
Deaths
8
Hospitalizations
How Dangerous Is Intentional product use issue From LOSARTAN?
Of the 67 reports, 1 (1.5%) resulted in death, 8 (11.9%) required hospitalization, and 3 (4.5%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOSARTAN. However, 67 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which LOSARTAN Alternatives Have Lower Intentional product use issue Risk?
LOSARTAN vs LOSARTAN\LOSARTAN
LOSARTAN vs LOTEPREDNOL ETABONATE
LOSARTAN vs LOTEPREDNOL ETABONATE\TOBRAMYCIN
LOSARTAN vs LOTILANER
LOSARTAN vs LOVASTATIN