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
118345452 11834545 2 F 20140115 20160201 20151214 20160210 PER US-JNJFOC-20151205223 JANSSEN 58.12 YR A F Y 0.00000 20160210 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
118345452 11834545 1 SS XARELTO RIVAROXABAN 1 Oral N 0 10 MG TABLET QD
118345452 11834545 2 PS XARELTO RIVAROXABAN 1 Oral N 22406 10 MG TABLET QD
118345452 11834545 3 C HYDROCODONE BITARTRATE AND ACETAMINOPHEN ACETAMINOPHENHYDROCODONE BITARTRATE 1 Oral EVERY 4 TO 6 HOUR AS NEEDED 0 1 DF TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
118345452 11834545 1 Deep vein thrombosis
118345452 11834545 2 Deep vein thrombosis
118345452 11834545 3 Pain

Outcome of event

Event ID CASEID OUTC COD
118345452 11834545 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
118345452 11834545 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
118345452 11834545 1 20140118 0
118345452 11834545 2 20140102 20140117 0
118345452 11834545 3 20140102 0