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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PROPOFOL Cause Recalled product administered? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Recalled product administered have been filed in association with PROPOFOL (Propofol). This represents 0.0% of all adverse event reports for PROPOFOL.

5
Reports of Recalled product administered with PROPOFOL
0.0%
of all PROPOFOL reports
0
Deaths
2
Hospitalizations

How Dangerous Is Recalled product administered From PROPOFOL?

Of the 5 reports, 2 (40.0%) required hospitalization.

Is Recalled product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROPOFOL. However, 5 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 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 PROPOFOL Alternatives Have Lower Recalled product administered Risk?

PROPOFOL vs PROPOXYPHENE PROPOFOL vs PROPOXYPHENE/ACETAMINOPHEN PROPOFOL vs PROPRANOLOL PROPOFOL vs PROPRANOLOL\PROPRANOLOL PROPOFOL vs PROPYLENE GLYCOL

Related Pages

PROPOFOL Full Profile All Recalled product administered Reports All Drugs Causing Recalled product administered PROPOFOL Demographics