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
127638321 12763832 1 I 20160208 20160907 20160920 20160920 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-074596 BRISTOL MYERS SQUIBB 86.39 YR M Y 0.00000 20160920 CN FR FR

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
127638321 12763832 1 PS COUMADINE WARFARIN SODIUM 1 Oral UNK U 9218 TABLET
127638321 12763832 2 SS INNOHEP TINZAPARIN SODIUM 1 Subcutaneous 14000 IU, QD Y 0 14000 IU QD
127638321 12763832 3 SS INNOHEP TINZAPARIN SODIUM 1 Subcutaneous 8000 IU, QD Y 0 8000 IU QD
127638321 12763832 4 C DIGOXIN. DIGOXIN 1 Unknown U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127638321 12763832 1 Arrhythmia
127638321 12763832 2 Product used for unknown indication
127638321 12763832 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127638321 12763832 HO
127638321 12763832 OT
127638321 12763832 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127638321 12763832 Abdominal pain
127638321 12763832 Abdominal wall haematoma
127638321 12763832 Anaemia
127638321 12763832 Bedridden
127638321 12763832 Fall
127638321 12763832 Hypotension
127638321 12763832 Malaise
127638321 12763832 Transfusion

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found