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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 VELETRI Cause Condition aggravated? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Condition aggravated have been filed in association with VELETRI. This represents 5.4% of all adverse event reports for VELETRI.

18
Reports of Condition aggravated with VELETRI
5.4%
of all VELETRI reports
8
Deaths
14
Hospitalizations

How Dangerous Is Condition aggravated From VELETRI?

Of the 18 reports, 8 (44.4%) resulted in death, 14 (77.8%) required hospitalization, and 2 (11.1%) were considered life-threatening.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for VELETRI. However, 18 reports have been filed with the FAERS database.

What Other Side Effects Does VELETRI Cause?

Dyspnoea (59) Death (48) Nausea (36) Pulmonary arterial hypertension (34) Pneumonia (33) Headache (30) Vomiting (27) Diarrhoea (26) Pain in jaw (23) Right ventricular failure (23)

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 VELETRI Alternatives Have Lower Condition aggravated Risk?

VELETRI vs VELIPARIB VELETRI vs VEMURAFENIB VELETRI vs VENETOCLAX VELETRI vs VENLAFAXINE VELETRI vs VENTAVIS

Related Pages

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