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
125153812 12515381 2 F 20151113 20160826 20160630 20160912 PER US-JNJFOC-20160522195 JANSSEN 58.35 YR A 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
125153812 12515381 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN 0 20 MG TABLET
125153812 12515381 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN 0 20 MG TABLET
125153812 12515381 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN;UNKNOWN;UNKNOWN;UNKNOWN 202439 20 MG TABLET
125153812 12515381 4 SS IBUPROFEN. IBUPROFEN 1 Unknown Y N 19012 TABLETS
125153812 12515381 5 SS IBUPROFEN. IBUPROFEN 1 Unknown Y N 19012 800 MG TABLETS
125153812 12515381 6 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 81 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125153812 12515381 1 Thrombosis prophylaxis
125153812 12515381 2 Cerebrovascular accident prophylaxis
125153812 12515381 3 Atrial fibrillation
125153812 12515381 5 Product used for unknown indication
125153812 12515381 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125153812 12515381 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125153812 12515381 Gastrointestinal haemorrhage
125153812 12515381 Renal 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
125153812 12515381 1 20151109 20151115 0
125153812 12515381 2 20151109 20151115 0
125153812 12515381 3 20151109 20151115 0