Does TRACLEER Cause Concomitant disease aggravated? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Concomitant disease aggravated have been filed in association with TRACLEER. This represents 0.5% of all adverse event reports for TRACLEER.
9
Reports of Concomitant disease aggravated with TRACLEER
0.5%
of all TRACLEER reports
5
Deaths
6
Hospitalizations
How Dangerous Is Concomitant disease aggravated From TRACLEER?
Of the 9 reports, 5 (55.6%) resulted in death, 6 (66.7%) required hospitalization, and 1 (11.1%) were considered life-threatening.
Is Concomitant disease aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TRACLEER. However, 9 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)
Condition aggravated (86)
Fall (79)
Fluid retention (65)
Dizziness (63)
Cardiac failure congestive (60)
Aspartate aminotransferase increased (59)
What Other Drugs Cause Concomitant disease aggravated?
SACUBITRIL\VALSARTAN (533)
SECUKINUMAB (461)
FINGOLIMOD (425)
MACITENTAN (286)
OMALIZUMAB (186)
SELEXIPAG (166)
METHOTREXATE (150)
RUXOLITINIB (142)
OCTREOTIDE (125)
BOSENTAN (123)
Which TRACLEER Alternatives Have Lower Concomitant disease aggravated Risk?
TRACLEER vs TRADJENTA
TRACLEER vs TRALOKINUMAB-LDRM
TRACLEER vs TRAMADOL
TRACLEER vs TRAMADOL\TRAMADOL
TRACLEER vs TRAMETINIB