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
123452283 12345228 3 F 201201 20160806 20160507 20160912 PER US-JNJFOC-20160409067 JANSSEN 81.50 YR E M Y 0.00000 20160912 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
123452283 12345228 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN 0 20 MG TABLET
123452283 12345228 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN 0 20 MG TABLET
123452283 12345228 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN 202439 20 MG TABLET
123452283 12345228 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123452283 12345228 1 Atrial fibrillation
123452283 12345228 2 Thrombosis prophylaxis
123452283 12345228 3 Cerebrovascular accident prophylaxis
123452283 12345228 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123452283 12345228 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123452283 12345228 Rectal haemorrhage
123452283 12345228 Upper gastrointestinal haemorrhage

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
123452283 12345228 1 20111219 20130530 0
123452283 12345228 2 20111219 20130530 0
123452283 12345228 3 20111219 20130530 0