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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 PRIALT Cause Device issue? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Device issue have been filed in association with PRIALT. This represents 22.6% of all adverse event reports for PRIALT.

12
Reports of Device issue with PRIALT
22.6%
of all PRIALT reports
0
Deaths
7
Hospitalizations

How Dangerous Is Device issue From PRIALT?

Of the 12 reports, 7 (58.3%) required hospitalization.

Is Device issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PRIALT. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does PRIALT Cause?

Confusional state (11) Hallucination, auditory (11) Pain (11) Hallucination (8) Mental status changes (7) Dizziness (6) Urinary retention (6) Anxiety (5) Drug ineffective (5) Drug withdrawal syndrome (5)

What Other Drugs Cause Device issue?

ADALIMUMAB (17,630) SOMATROPIN (5,131) PEGFILGRASTIM (5,071) ETANERCEPT (4,143) INSULIN GLARGINE (3,175) EXENATIDE (2,862) LEVONORGESTREL (2,623) CARBIDOPA\LEVODOPA (2,574) GOLIMUMAB (1,827) USTEKINUMAB (1,716)

Related Pages

PRIALT Full Profile All Device issue Reports All Drugs Causing Device issue PRIALT Demographics