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
123143902 12314390 2 F 201312 20160727 20160428 20160805 EXP US-JNJFOC-20160423125 JANSSEN 81.16 YR E F Y 0.00000 20160805 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
123143902 12314390 1 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
123143902 12314390 2 SS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 0 20 MG TABLET
123143902 12314390 3 PS XARELTO RIVAROXABAN 1 Oral Y N UNKNOWN 202439 20 MG TABLET
123143902 12314390 4 SS TYLENOL ACETAMINOPHEN 1 Oral N 19872 TABLETS
123143902 12314390 5 SS TYLENOL ACETAMINOPHEN 1 Oral N 19872 325 MG TABLETS
123143902 12314390 6 SS ASPIRIN. ASPIRIN 1 Oral 0 81 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123143902 12314390 1 Thrombosis prophylaxis
123143902 12314390 2 Cerebrovascular accident prophylaxis
123143902 12314390 3 Atrial fibrillation
123143902 12314390 5 Product used for unknown indication
123143902 12314390 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123143902 12314390 DE
123143902 12314390 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
123143902 12314390 Acute kidney injury
123143902 12314390 Gastrointestinal haemorrhage
123143902 12314390 International normalised ratio increased

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
123143902 12314390 1 20130421 20131203 0
123143902 12314390 2 20130421 20131203 0
123143902 12314390 3 20130421 20131203 0