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
126472701 12647270 1 I 20140721 20160506 20160812 20160812 EXP US-BAYER-2016-093375 BAYER 60.00 YR A M Y 0.00000 20160812 OT 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
126472701 12647270 1 SS XARELTO RIVAROXABAN 1 Oral UNK 12560 MG N UNKNOWN 0 20 MG FILM-COATED TABLET QD
126472701 12647270 2 SS XARELTO RIVAROXABAN 1 12560 MG N 0 FILM-COATED TABLET
126472701 12647270 3 PS ACETYLSALICYLIC ACID (} 100 mg) ASPIRIN 1 Oral 162 MG, QD 999999 162 MG TABLET QD
126472701 12647270 4 SS PLAVIX CLOPIDOGREL BISULFATE 1 Oral 75 MG, QD 0 75 MG QD
126472701 12647270 5 SS ENOXAPARIN SODIUM. ENOXAPARIN SODIUM 1 Oral 40 MG, QD U 0 40 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126472701 12647270 1 Deep vein thrombosis
126472701 12647270 2 Embolism venous
126472701 12647270 3 Product used for unknown indication
126472701 12647270 4 Product used for unknown indication
126472701 12647270 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126472701 12647270 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126472701 12647270 Anaemia
126472701 12647270 Renal 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
126472701 12647270 1 20121101 20150601 0
126472701 12647270 3 201408 0
126472701 12647270 4 201408 0