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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 ENZALUTAMIDE Cause Product container issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product container issue have been filed in association with ENZALUTAMIDE (Xtandi). This represents 0.0% of all adverse event reports for ENZALUTAMIDE.

5
Reports of Product container issue with ENZALUTAMIDE
0.0%
of all ENZALUTAMIDE reports
0
Deaths
1
Hospitalizations

How Dangerous Is Product container issue From ENZALUTAMIDE?

Of the 5 reports, 1 (20.0%) required hospitalization.

Is Product container issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ENZALUTAMIDE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does ENZALUTAMIDE Cause?

Fatigue (8,891) Death (6,680) Malignant neoplasm progression (4,696) Prostatic specific antigen increased (3,731) Asthenia (3,589) Drug ineffective (3,468) Hot flush (3,144) Decreased appetite (3,069) Nausea (2,898) Dizziness (2,776)

What Other Drugs Cause Product container issue?

CYCLOSPORINE (910) MINOXIDIL (556) MOMETASONE FUROATE (450) FORMOTEROL\MOMETASONE FUROATE (375) LIFITEGRAST (244) ALBUTEROL (192) LATANOPROST (158) CARBOXYMETHYLCELLULOSE\GLYCERIN (123) BRIMONIDINE (121) ACETAMINOPHEN (118)

Which ENZALUTAMIDE Alternatives Have Lower Product container issue Risk?

ENZALUTAMIDE vs EPCORITAMAB ENZALUTAMIDE vs EPCORITAMAB-BYSP ENZALUTAMIDE vs EPERISONE ENZALUTAMIDE vs EPHEDRINE ENZALUTAMIDE vs EPINASTINE

Related Pages

ENZALUTAMIDE Full Profile All Product container issue Reports All Drugs Causing Product container issue ENZALUTAMIDE Demographics