Does TRACLEER Cause Condition aggravated? 86 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 86 reports of Condition aggravated have been filed in association with TRACLEER. This represents 4.6% of all adverse event reports for TRACLEER.
86
Reports of Condition aggravated with TRACLEER
4.6%
of all TRACLEER reports
46
Deaths
55
Hospitalizations
How Dangerous Is Condition aggravated From TRACLEER?
Of the 86 reports, 46 (53.5%) resulted in death, 55 (64.0%) required hospitalization, and 8 (9.3%) 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 TRACLEER. However, 86 reports have been filed with the FAERS database.
What Other Side Effects Does TRACLEER Cause?
Death (382)
Dyspnoea (229)
Pulmonary arterial hypertension (127)
Pneumonia (121)
Fall (79)
Fluid retention (65)
Dizziness (63)
Cardiac failure congestive (60)
Aspartate aminotransferase increased (59)
Fatigue (59)
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 TRACLEER Alternatives Have Lower Condition aggravated Risk?
TRACLEER vs TRADJENTA
TRACLEER vs TRALOKINUMAB-LDRM
TRACLEER vs TRAMADOL
TRACLEER vs TRAMADOL\TRAMADOL
TRACLEER vs TRAMETINIB