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
125122322 12512232 2 F 20141203 20160812 20160630 20160912 PER US-JNJFOC-20160610432 JANSSEN 70.82 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
125122322 12512232 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125122322 12512232 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
125122322 12512232 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
125122322 12512232 4 SS ASPIRIN. ASPIRIN 1 Unknown U 0 UNSPECIFIED
125122322 12512232 5 SS EFFIENT PRASUGREL HYDROCHLORIDE 1 Oral U 0 10 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125122322 12512232 1 Atrial fibrillation
125122322 12512232 2 Thrombosis prophylaxis
125122322 12512232 3 Cerebrovascular accident prophylaxis
125122322 12512232 4 Product used for unknown indication
125122322 12512232 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125122322 12512232 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125122322 12512232 Haemoptysis

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
125122322 12512232 1 20130716 20141203 0
125122322 12512232 2 20130716 20141203 0
125122322 12512232 3 20130716 20141203 0