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
125157712 12515771 2 F 20131007 20160912 20160630 20160921 PER US-JNJFOC-20160523075 JANSSEN 59.13 YR A M Y 0.00000 20160921 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
125157712 12515771 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125157712 12515771 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125157712 12515771 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
125157712 12515771 4 SS IBUPROFEN. IBUPROFEN 1 Oral Y N 17463 TABLETS
125157712 12515771 5 SS ASPIRIN. ASPIRIN 1 Oral Y 0 324 MG CHEWABLE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125157712 12515771 1 Atrial fibrillation
125157712 12515771 2 Thrombosis prophylaxis
125157712 12515771 3 Cerebrovascular accident prophylaxis
125157712 12515771 4 Product used for unknown indication
125157712 12515771 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125157712 12515771 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125157712 12515771 Upper 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
125157712 12515771 1 20130629 20131007 0
125157712 12515771 2 20130629 20131007 0
125157712 12515771 3 20130629 20131007 0