The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
5040237 6046255 I 5040237-4 20060409 20060623 20060630 EXP US-JNJFOC-20060501813 CENTOCOR, INC. M Y 20060630 MD UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
5040237 1007430324 SS REMICADE 1
5040237 1007430325 SS REMICADE 1
5040237 1007430326 SS REMICADE 1
5040237 1007430327 SS REMICADE 1
5040237 1007430328 SS REMICADE 1
5040237 1007430329 SS REMICADE 1
5040237 1007430330 SS REMICADE 1
5040237 1007430331 PS REMICADE 1
5040237 1007430332 SS REMICADE 1
5040237 1007430333 C TEGRETOL 1 ORAL
5040237 1007430334 C ALLEGRA 1 ORAL
5040237 1007430335 C NASONEX 1 NASAL
5040237 1007430336 C ROBINUL 1 ORAL
5040237 1007430337 C IMODIUM 1 ORAL
5040237 1007430338 C PREDNISONE 1 ORAL
5040237 1007430339 C ASACOL 1 ORAL
5040237 1007430340 C PROZAC 1 ORAL

Indications of drugs used

Event ID DRUG SEQ INDI PT
5040237 1007430332 COLITIS ULCERATIVE
5040237 1007430333 EPILEPSY
5040237 1007430334 SINUSITIS
5040237 1007430335 SINUSITIS
5040237 1007430336 COLITIS ULCERATIVE
5040237 1007430337 COLITIS ULCERATIVE
5040237 1007430338 COLITIS ULCERATIVE
5040237 1007430339 COLITIS ULCERATIVE
5040237 1007430340 DEPRESSION

Outcome of event

Event ID OUTC COD
5040237 HO

Reactions reported

Event ID PT
5040237 DYSPNOEA
5040237 ERYTHEMA MULTIFORME
5040237 LYMPHADENOPATHY
5040237 SARCOIDOSIS

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found