Does PROPOFOL Cause Product use in unapproved indication? 367 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 367 reports of Product use in unapproved indication have been filed in association with PROPOFOL (Propofol). This represents 2.3% of all adverse event reports for PROPOFOL.
367
Reports of Product use in unapproved indication with PROPOFOL
2.3%
of all PROPOFOL reports
55
Deaths
155
Hospitalizations
How Dangerous Is Product use in unapproved indication From PROPOFOL?
Of the 367 reports, 55 (15.0%) resulted in death, 155 (42.2%) required hospitalization, and 73 (19.9%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROPOFOL. However, 367 reports have been filed with the FAERS database.
What Other Side Effects Does PROPOFOL Cause?
Drug ineffective (1,627)
Anaphylactic shock (1,494)
Hypotension (1,388)
Off label use (889)
Anaphylactic reaction (862)
Cardiac arrest (758)
Bradycardia (470)
Tachycardia (464)
Propofol infusion syndrome (420)
Foetal exposure during pregnancy (389)
What Other Drugs Cause Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which PROPOFOL Alternatives Have Lower Product use in unapproved indication Risk?
PROPOFOL vs PROPOXYPHENE
PROPOFOL vs PROPOXYPHENE/ACETAMINOPHEN
PROPOFOL vs PROPRANOLOL
PROPOFOL vs PROPRANOLOL\PROPRANOLOL
PROPOFOL vs PROPYLENE GLYCOL