Does FUROSEMIDE Cause Wrong technique in product usage process? 165 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 165 reports of Wrong technique in product usage process have been filed in association with FUROSEMIDE (Furosemide). This represents 0.3% of all adverse event reports for FUROSEMIDE.
165
Reports of Wrong technique in product usage process with FUROSEMIDE
0.3%
of all FUROSEMIDE reports
6
Deaths
70
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FUROSEMIDE?
Of the 165 reports, 6 (3.6%) resulted in death, 70 (42.4%) required hospitalization, and 9 (5.5%) 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 FUROSEMIDE. However, 165 reports have been filed with the FAERS database.
What Other Side Effects Does FUROSEMIDE Cause?
Acute kidney injury (7,984)
Hypotension (4,468)
Dyspnoea (3,559)
Fall (3,410)
Drug ineffective (3,297)
Hyponatraemia (3,127)
Hypokalaemia (2,503)
Dehydration (2,195)
Off label use (2,147)
Fatigue (2,107)
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 FUROSEMIDE Alternatives Have Lower Wrong technique in product usage process Risk?
FUROSEMIDE vs FUROSEMIDE\SPIRONOLACTONE
FUROSEMIDE vs FUSIDATE
FUROSEMIDE vs FUSIDIC ACID
FUROSEMIDE vs FUTIBATINIB
FUROSEMIDE vs GABAPENTIN