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
123447233 12344723 3 F 201403 20160620 20160507 20160912 PER US-JNJFOC-20160328588 JANSSEN 77.40 YR E F 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
123447233 12344723 1 SS XARELTO RIVAROXABAN 1 Oral DOSE: 15 AND 20 MG Y N UNKNOWN;UNKNOWN 0 TABLET
123447233 12344723 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN 0 20 MG TABLET
123447233 12344723 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN 22406 20 MG TABLET
123447233 12344723 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral Y 0 75 MG UNSPECIFIED
123447233 12344723 5 SS ASPIRIN. ASPIRIN 1 Oral Y 0 81 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123447233 12344723 1 Thrombosis
123447233 12344723 2 Thrombosis
123447233 12344723 3 Thrombosis
123447233 12344723 4 Product used for unknown indication
123447233 12344723 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123447233 12344723 OT
123447233 12344723 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123447233 12344723 Gastrointestinal haemorrhage
123447233 12344723 Internal haemorrhage
123447233 12344723 Lower 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
123447233 12344723 1 201310 201310 0
123447233 12344723 2 201309 201310 0
123447233 12344723 3 2013 201405 0
123447233 12344723 4 201405 0
123447233 12344723 5 201406 0