Does RISPERDAL CONSTA Cause Investigation? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Investigation have been filed in association with RISPERDAL CONSTA. This represents 3.6% of all adverse event reports for RISPERDAL CONSTA.
5
Reports of Investigation with RISPERDAL CONSTA
3.6%
of all RISPERDAL CONSTA reports
0
Deaths
5
Hospitalizations
How Dangerous Is Investigation From RISPERDAL CONSTA?
Of the 5 reports, 5 (100.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Investigation Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RISPERDAL CONSTA. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does RISPERDAL CONSTA Cause?
Death (13)
Psychotic disorder (10)
Hospitalisation (9)
Drug ineffective (8)
Weight increased (7)
Tremor (6)
Anxiety (5)
Drug dose omission (5)
Myocardial infarction (5)
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 RISPERDAL CONSTA Alternatives Have Lower Investigation Risk?
RISPERDAL CONSTA vs RISPERIDONE
RISPERDAL CONSTA vs RITALIN
RISPERDAL CONSTA vs RITLECITINIB
RISPERDAL CONSTA vs RITODRINE
RISPERDAL CONSTA vs RITONAVIR