The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
109927953 10992795 3 F 20131223 20160623 20150406 20160701 EXP US-JNJFOC-20140104859 JANSSEN 49.27 YR A M Y 110.22000 KG 20160701 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
109927953 10992795 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 552.2 MG, ACCORDING TO PATIENT'S BODT WEIGHT.??THE PATIENT RECEIVED 600 MG.??WEEK 0 AND 2 Y U 13FO81P1;DCM17011P1;13DO83P1 0 5 MG/KG LYOPHILIZED POWDER
109927953 10992795 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) 552.2 MG, ACCORDING TO PATIENT'S BODT WEIGHT.??THE PATIENT RECEIVED 600 MG. Y U 13FO81P1;DCM17011P1;13DO83P1 103772 5 MG/KG LYOPHILIZED POWDER
109927953 10992795 3 C LANTUS INSULIN GLARGINE 1 Unknown 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
109927953 10992795 1 Psoriatic arthropathy
109927953 10992795 2 Psoriatic arthropathy
109927953 10992795 3 Diabetes mellitus

Outcome of event

Event ID CASEID OUTC COD
109927953 10992795 HO
109927953 10992795 DS
109927953 10992795 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
109927953 10992795 Decubitus ulcer
109927953 10992795 Myelopathy
109927953 10992795 Weight decreased

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
109927953 10992795 1 20131202 0
109927953 10992795 2 20131216 0