Does LOSARTAN Cause Recalled product administered? 141 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 141 reports of Recalled product administered have been filed in association with LOSARTAN (Losartan Potassium). This represents 0.6% of all adverse event reports for LOSARTAN.
141
Reports of Recalled product administered with LOSARTAN
0.6%
of all LOSARTAN reports
3
Deaths
17
Hospitalizations
How Dangerous Is Recalled product administered From LOSARTAN?
Of the 141 reports, 3 (2.1%) resulted in death, 17 (12.1%) required hospitalization, and 18 (12.8%) were considered life-threatening.
Is Recalled product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOSARTAN. However, 141 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 administered?
RAMIPRIL (1,028)
LISINOPRIL (744)
PENICILLIN G BENZATHINE (500)
LEVOTHYROXINE (406)
HUMAN IMMUNOGLOBULIN G (382)
VARENICLINE (381)
VALSARTAN (267)
QUINAPRIL (243)
TRIAMCINOLONE ACETONIDE (222)
RANITIDINE (204)
Which LOSARTAN Alternatives Have Lower Recalled product administered Risk?
LOSARTAN vs LOSARTAN\LOSARTAN
LOSARTAN vs LOTEPREDNOL ETABONATE
LOSARTAN vs LOTEPREDNOL ETABONATE\TOBRAMYCIN
LOSARTAN vs LOTILANER
LOSARTAN vs LOVASTATIN