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
127981831 12798183 1 I 20160610 20160923 20160930 20160930 EXP FR-SA-2016SA179927 AVENTIS 63.00 YR A F Y 0.00000 20160930 OT FR FR

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
127981831 12798183 1 PS IMMUCYST BACILLUS CALMETTE-GUERIN SUBSTRAIN CONNAUGHT LIVE ANTIGEN 1 Intracoronary 1/ 0.1429 DOSAGE FORM 1 DOSAGE FORM IN 1 WEEK. D UNKNOWN 103943
127981831 12798183 2 SS IMMUCYST BACILLUS CALMETTE-GUERIN SUBSTRAIN CONNAUGHT LIVE ANTIGEN 1 Intracoronary 1/ 0.1429 DOSAGE FORM 1 DOSAGE FORM IN 1 WEEK. D UNKNOWN 103943

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127981831 12798183 1 Bladder cancer
127981831 12798183 2 Bladder cancer

Outcome of event

Event ID CASEID OUTC COD
127981831 12798183 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127981831 12798183 Arthralgia
127981831 12798183 Disseminated Bacillus Calmette-Guerin infection
127981831 12798183 Polyarthritis
127981831 12798183 Pyrexia
127981831 12798183 Spinal pain
127981831 12798183 Synovitis

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
127981831 12798183 1 20160610 20160610 0
127981831 12798183 2 20160607 20160607 0