Does ZICONOTIDE Cause Device issue? 296 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 296 reports of Device issue have been filed in association with ZICONOTIDE (PRIALT). This represents 16.4% of all adverse event reports for ZICONOTIDE.
296
Reports of Device issue with ZICONOTIDE
16.4%
of all ZICONOTIDE reports
4
Deaths
46
Hospitalizations
How Dangerous Is Device issue From ZICONOTIDE?
Of the 296 reports, 4 (1.4%) resulted in death, 46 (15.5%) required hospitalization, and 3 (1.0%) were considered life-threatening.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ZICONOTIDE. However, 296 reports have been filed with the FAERS database.
What Other Side Effects Does ZICONOTIDE Cause?
Off label use (289)
Pain (248)
Drug ineffective (210)
Nausea (144)
Hallucination (121)
Confusional state (113)
Hallucination, auditory (98)
Dizziness (95)
Headache (91)
Malaise (70)
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)
Which ZICONOTIDE Alternatives Have Lower Device issue Risk?
ZICONOTIDE vs ZIDOVUDINE
ZICONOTIDE vs ZILEUTON
ZICONOTIDE vs ZILUCOPLAN
ZICONOTIDE vs ZIMBERELIMAB
ZICONOTIDE vs ZINC