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
122315433 12231543 3 F 20140601 20160714 20160401 20160725 EXP US-JNJFOC-20160317079 JANSSEN 80.40 YR E M Y 0.00000 20160725 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
122315433 12231543 1 SS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 0 15 MG TABLET
122315433 12231543 2 SS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 0 15 MG TABLET
122315433 12231543 3 PS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 202439 15 MG TABLET
122315433 12231543 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Unknown U 0 UNSPECIFIED
122315433 12231543 5 SS ASPIRIN. ASPIRIN 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
122315433 12231543 1 Thrombosis prophylaxis
122315433 12231543 2 Cerebrovascular accident prophylaxis
122315433 12231543 3 Atrial fibrillation
122315433 12231543 4 Atrial fibrillation
122315433 12231543 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
122315433 12231543 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
122315433 12231543 Fall
122315433 12231543 Haematoma
122315433 12231543 Haemorrhage
122315433 12231543 Nasal septum haematoma
122315433 12231543 Rhabdomyolysis
122315433 12231543 Subdural haematoma
122315433 12231543 Subgaleal haematoma

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
122315433 12231543 1 20130709 20140607 0
122315433 12231543 2 20130709 20140607 0
122315433 12231543 3 20130709 20140607 0