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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 REMODULIN Cause Unevaluable event? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Unevaluable event have been filed in association with REMODULIN. This represents 0.9% of all adverse event reports for REMODULIN.

6
Reports of Unevaluable event with REMODULIN
0.9%
of all REMODULIN reports
1
Deaths
3
Hospitalizations

How Dangerous Is Unevaluable event From REMODULIN?

Of the 6 reports, 1 (16.7%) resulted in death, 3 (50.0%) required hospitalization.

Is Unevaluable event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REMODULIN. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does REMODULIN Cause?

Death (95) Dyspnoea (79) Device related infection (64) Drug dose omission (42) Nausea (32) Headache (30) Diarrhoea (28) Pulmonary arterial hypertension (28) Vomiting (28) Fluid retention (27)

What Other Drugs Cause Unevaluable event?

ADALIMUMAB (4,242) ETANERCEPT (3,902) LENALIDOMIDE (3,331) OXYCODONE (3,145) AMBRISENTAN (2,336) SODIUM OXYBATE (2,328) CARBIDOPA\LEVODOPA (1,632) DUPILUMAB (1,410) MORPHINE (1,161) ACETAMINOPHEN\HYDROCODONE (1,118)

Which REMODULIN Alternatives Have Lower Unevaluable event Risk?

REMODULIN vs REPAGLINIDE REMODULIN vs REPOTRECTINIB REMODULIN vs REQUIP REMODULIN vs RESLIZUMAB REMODULIN vs RESMETIROM

Related Pages

REMODULIN Full Profile All Unevaluable event Reports All Drugs Causing Unevaluable event REMODULIN Demographics