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
127330291 12733029 1 I 20140605 20160630 20160912 20160912 PER US-JNJFOC-20160703256 JANSSEN 77.58 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
127330291 12733029 1 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
127330291 12733029 2 SS XARELTO RIVAROXABAN 1 Oral Y N 0 20 MG TABLET QD
127330291 12733029 3 PS XARELTO RIVAROXABAN 1 Oral Y N 202439 20 MG TABLET QD
127330291 12733029 4 SS COUMADIN WARFARIN SODIUM 1 Unknown Y 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127330291 12733029 1 Atrial fibrillation
127330291 12733029 2 Thrombosis prophylaxis
127330291 12733029 3 Cerebrovascular accident prophylaxis
127330291 12733029 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127330291 12733029 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127330291 12733029 Haematoma
127330291 12733029 Haematuria
127330291 12733029 Haemorrhagic arteriovenous malformation

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
127330291 12733029 1 20140429 20140904 0
127330291 12733029 2 20140429 20140904 0
127330291 12733029 3 20140429 20140904 0