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
127325081 12732508 1 I 20130719 20160617 20160912 20160912 PER US-JNJFOC-20160617149 JANSSEN 66.86 YR E F Y 54.43000 KG 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
127325081 12732508 1 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 20 MG TABLET
127325081 12732508 2 SS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 0 20 MG TABLET
127325081 12732508 3 PS XARELTO RIVAROXABAN 1 Oral U U UNKNOWN 202439 20 MG TABLET
127325081 12732508 4 SS MOTRIN IBUPROFEN 1 Unknown U U 19012 UNSPECIFIED
127325081 12732508 5 SS ASPIRIN. ASPIRIN 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127325081 12732508 1 Embolism
127325081 12732508 2 Atrial fibrillation
127325081 12732508 3 Cerebrovascular accident prophylaxis
127325081 12732508 4 Back pain
127325081 12732508 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127325081 12732508 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127325081 12732508 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
127325081 12732508 1 20121210 0
127325081 12732508 2 20121210 0
127325081 12732508 3 20121210 0