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
124172942 12417294 2 F 2011 20160701 20160530 20160707 EXP US-JNJFOC-20130811998 JANSSEN 0.00 A F Y 58.97000 KG 20160707 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
124172942 12417294 1 SS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) Y N UNKNOWN 0 LYOPHILIZED POWDER
124172942 12417294 2 PS REMICADE INFLIXIMAB 1 Intravenous (not otherwise specified) Y N UNKNOWN 103772 LYOPHILIZED POWDER
124172942 12417294 3 C LOSARTAN. LOSARTAN 1 Oral 60-12.5MG 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
124172942 12417294 1 Rheumatoid arthritis
124172942 12417294 2 Rheumatoid arthritis
124172942 12417294 3 Blood pressure measurement

Outcome of event

Event ID CASEID OUTC COD
124172942 12417294 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
124172942 12417294 Abasia
124172942 12417294 Balance disorder
124172942 12417294 Contusion
124172942 12417294 Fatigue
124172942 12417294 Gait disturbance
124172942 12417294 Joint swelling
124172942 12417294 Therapeutic response 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
124172942 12417294 1 2011 2013 0
124172942 12417294 2 2013 2013 0