Does REMICADE Cause Investigation? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Investigation have been filed in association with REMICADE. This represents 0.8% of all adverse event reports for REMICADE.
26
Reports of Investigation with REMICADE
0.8%
of all REMICADE reports
0
Deaths
26
Hospitalizations
How Dangerous Is Investigation From REMICADE?
Of the 26 reports, 26 (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 REMICADE. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does REMICADE Cause?
Infusion related reaction (313)
Crohn's disease (193)
Drug ineffective (157)
Dyspnoea (141)
Exposure during pregnancy (96)
Arthralgia (95)
Nausea (85)
Pain (84)
Vomiting (81)
Malaise (80)
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 REMICADE Alternatives Have Lower Investigation Risk?
REMICADE vs REMIFENTANIL
REMICADE vs REMIMAZOLAM
REMICADE vs REMODULIN
REMICADE vs REPAGLINIDE
REMICADE vs REPOTRECTINIB