Does LOSARTAN Cause Wrong technique in product usage process? 219 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 219 reports of Wrong technique in product usage process have been filed in association with LOSARTAN (Losartan Potassium). This represents 1.0% of all adverse event reports for LOSARTAN.
219
Reports of Wrong technique in product usage process with LOSARTAN
1.0%
of all LOSARTAN reports
7
Deaths
44
Hospitalizations
How Dangerous Is Wrong technique in product usage process From LOSARTAN?
Of the 219 reports, 7 (3.2%) resulted in death, 44 (20.1%) required hospitalization, and 16 (7.3%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for LOSARTAN. However, 219 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which LOSARTAN Alternatives Have Lower Wrong technique in product usage process Risk?
LOSARTAN vs LOSARTAN\LOSARTAN
LOSARTAN vs LOTEPREDNOL ETABONATE
LOSARTAN vs LOTEPREDNOL ETABONATE\TOBRAMYCIN
LOSARTAN vs LOTILANER
LOSARTAN vs LOVASTATIN