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
127419801 12741980 1 I 201311 20160518 20160914 20160914 EXP US-BAYER-2016-104704 BAYER 31.00 YR A M Y 101.10000 KG 20160914 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
127419801 12741980 1 SS XARELTO RIVAROXABAN 1 Oral 15 MG, UNK U UNKNOWN 0 15 MG FILM-COATED TABLET
127419801 12741980 2 SS XARELTO RIVAROXABAN 1 Oral 20 MG, UNK U UNKNOWN 0 20 MG FILM-COATED TABLET
127419801 12741980 3 SS XARELTO RIVAROXABAN 1 U 0 FILM-COATED TABLET
127419801 12741980 4 SS LOVENOX ENOXAPARIN SODIUM 1 Unknown 100 MG, UNK U 0 100 MG
127419801 12741980 5 PS ACETYLSALICYLIC ACID({=100 mg) ASPIRIN 1 Oral 324 MG, UNK U 999999 324 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127419801 12741980 1 Pulmonary embolism
127419801 12741980 2 Thrombosis prophylaxis
127419801 12741980 3 Embolism venous
127419801 12741980 4 Product used for unknown indication
127419801 12741980 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127419801 12741980 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127419801 12741980 Chest pain
127419801 12741980 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
127419801 12741980 1 20130913 20141003 0
127419801 12741980 2 20131004 0
127419801 12741980 4 20130913 0
127419801 12741980 5 20130913 0