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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 Condition aggravated? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Condition aggravated have been filed in association with REMODULIN. This represents 1.6% of all adverse event reports for REMODULIN.

11
Reports of Condition aggravated with REMODULIN
1.6%
of all REMODULIN reports
4
Deaths
7
Hospitalizations

How Dangerous Is Condition aggravated From REMODULIN?

Of the 11 reports, 4 (36.4%) resulted in death, 7 (63.6%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REMODULIN. However, 11 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 Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which REMODULIN Alternatives Have Lower Condition aggravated Risk?

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

Related Pages

REMODULIN Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated REMODULIN Demographics