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
127181261 12718126 1 I 201406 20160715 20160906 20160906 EXP US-JNJFOC-20160714647 JANSSEN 67.03 YR E M Y 0.00000 20160906 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
127181261 12718126 1 SS XARELTO RIVAROXABAN 1 Oral N 0 TABLET
127181261 12718126 2 SS XARELTO RIVAROXABAN 1 Oral 15-20 MG N 0 TABLET
127181261 12718126 3 SS XARELTO RIVAROXABAN 1 Oral N 0 TABLET
127181261 12718126 4 PS XARELTO RIVAROXABAN 1 Oral 15-20 MG N 22406 TABLET
127181261 12718126 5 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral 0 75 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127181261 12718126 1 Deep vein thrombosis
127181261 12718126 2 Deep vein thrombosis
127181261 12718126 3 Atrial fibrillation
127181261 12718126 4 Atrial fibrillation
127181261 12718126 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127181261 12718126 DE
127181261 12718126 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127181261 12718126 Cerebral haemorrhage
127181261 12718126 Cerebrovascular accident
127181261 12718126 Contusion
127181261 12718126 Head injury
127181261 12718126 Lower gastrointestinal haemorrhage
127181261 12718126 Subarachnoid 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
127181261 12718126 1 201407 0
127181261 12718126 2 201404 20140622 0
127181261 12718126 3 201407 0
127181261 12718126 4 201404 20140622 0