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
125122172 12512217 2 F 20140405 20160804 20160630 20160912 PER US-JNJFOC-20160509718 JANSSEN 72.82 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
125122172 12512217 1 SS XARELTO RIVAROXABAN 1 Oral VARYING 15-20 MG Y N UNKNOWN 0 TABLET
125122172 12512217 2 SS XARELTO RIVAROXABAN 1 Oral VARYING 15-20 MG Y N UNKNOWN 0 TABLET
125122172 12512217 3 PS XARELTO RIVAROXABAN 1 Oral VARYING 15-20 MG Y N UNKNOWN 202439 TABLET
125122172 12512217 4 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
125122172 12512217 5 SS IBUPROFEN. IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125122172 12512217 1 Atrial fibrillation
125122172 12512217 2 Thrombosis prophylaxis
125122172 12512217 3 Cerebrovascular accident prophylaxis
125122172 12512217 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125122172 12512217 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125122172 12512217 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
125122172 12512217 1 20131204 20140405 0
125122172 12512217 2 20131204 20140405 0
125122172 12512217 3 20131204 20140405 0