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
127316332 12731633 2 F 20140703 20160914 20160912 20160921 PER US-JNJFOC-20160620328 JANSSEN 75.62 YR E F Y 0.00000 20160921 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
127316332 12731633 1 SS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 0 15 MG TABLET
127316332 12731633 2 PS XARELTO RIVAROXABAN 1 Oral Y U UNKNOWN 22406 15 MG TABLET
127316332 12731633 3 SS COUMADIN WARFARIN SODIUM 1 Oral DOSE: 5MG, 10MG Y 0 TABLET
127316332 12731633 4 SS LOVENOX ENOXAPARIN SODIUM 1 Subcutaneous Y 0 80 MG INJECTION
127316332 12731633 5 SS ASPIRIN. ASPIRIN 1 Unknown Y 0 81 MG UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127316332 12731633 1 Deep vein thrombosis
127316332 12731633 2 Deep vein thrombosis
127316332 12731633 3 Deep vein thrombosis
127316332 12731633 4 Product used for unknown indication
127316332 12731633 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127316332 12731633 HO
127316332 12731633 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127316332 12731633 Haemoptysis
127316332 12731633 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
127316332 12731633 1 201411 0
127316332 12731633 2 20140508 201407 0