Does PROMACTA Cause Investigation? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Investigation have been filed in association with PROMACTA. This represents 5.7% of all adverse event reports for PROMACTA.
17
Reports of Investigation with PROMACTA
5.7%
of all PROMACTA reports
1
Deaths
17
Hospitalizations
How Dangerous Is Investigation From PROMACTA?
Of the 17 reports, 1 (5.9%) resulted in death, 17 (100.0%) required hospitalization.
Is Investigation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PROMACTA. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does PROMACTA Cause?
Platelet count decreased (34)
Death (29)
Drug ineffective (26)
Nausea (16)
Diarrhoea (13)
Headache (12)
Platelet count increased (12)
Treatment noncompliance (12)
Fatigue (11)
Abdominal pain upper (9)
What Other Drugs Cause Investigation?
ARANESP (403)
NEULASTA (371)
XGEVA (115)
FLUTICASONE\SALMETEROL (96)
DARBEPOETIN ALFA (86)
ADVAIR (77)
DENOSUMAB (65)
ADVAIR HFA (51)
ALBUTEROL (51)
VENTOLIN (47)
Which PROMACTA Alternatives Have Lower Investigation Risk?
PROMACTA vs PROMAZINE
PROMACTA vs PROMETHAZINE
PROMACTA vs PROMETHAZINE\PROMETHAZINE
PROMACTA vs PROMETHAZINE\THIOUREA
PROMACTA vs PROPAFENONE