The Safety Rates Drug Report

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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
125979421 12597942 1 I 20160117 20160712 20160726 20160726 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-BMS-2016-057906 BRISTOL MYERS SQUIBB 75.98 YR M Y 97.70000 KG 20160726 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
125979421 12597942 1 PS COUMADINE WARFARIN SODIUM 1 Oral UNK, QD U 9218 TABLET QD
125979421 12597942 2 SS COVERSYL /00790702/ PERINDOPRIL 1 Oral UNK UNK, QD U 0 QD
125979421 12597942 3 SS LASILIX /00032601/ FUROSEMIDE 1 Oral 1 DF, UNK U 0 1 DF
125979421 12597942 4 SS GENTAMYCIN /00047101/ GENTAMICIN 1 Unknown UNK Y 0
125979421 12597942 5 SS CLOXACILLIN CLOXACILLIN 1 Unknown UNK U 0
125979421 12597942 6 C CORDARON AMIODARONE HYDROCHLORIDE 1 Unknown 200 MG, QD U 0 200 MG QD
125979421 12597942 7 C BISOPROLOL BISOPROLOL 1 Unknown 2.5 MG, QD U 0 2.5 MG QD
125979421 12597942 8 C SPECIAFOLDINE FOLIC ACID 1 Unknown 5 MG, UNK U 0 5 MG
125979421 12597942 9 C TARDYFERON FERROUS SULFATE 1 Unknown 80 MG, BID U 0 80 MG BID
125979421 12597942 10 C PRAVASTATIN. PRAVASTATIN 1 Unknown UNK, QD U 0 QD
125979421 12597942 11 C LEVOTHYROX LEVOTHYROXINE 1 Unknown 100 ?G, QD U 0 100 UG QD
125979421 12597942 12 C DIFFU-K POTASSIUM CHLORIDE 1 Unknown 600 MG, QD U 0 600 MG QD
125979421 12597942 13 C NOVONORM REPAGLINIDE 1 Unknown 0.5 MG, QD U 0 .5 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125979421 12597942 1 Atrial fibrillation
125979421 12597942 2 Hypertension
125979421 12597942 3 Product used for unknown indication
125979421 12597942 4 Product used for unknown indication
125979421 12597942 5 Product used for unknown indication
125979421 12597942 6 Atrial fibrillation
125979421 12597942 7 Product used for unknown indication
125979421 12597942 8 Product used for unknown indication
125979421 12597942 9 Product used for unknown indication
125979421 12597942 10 Product used for unknown indication
125979421 12597942 11 Product used for unknown indication
125979421 12597942 12 Product used for unknown indication
125979421 12597942 13 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125979421 12597942 OT
125979421 12597942 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125979421 12597942 Acute kidney injury
125979421 12597942 Arthritis bacterial
125979421 12597942 Dialysis
125979421 12597942 International normalised ratio increased
125979421 12597942 Overdose
125979421 12597942 Transfusion

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
125979421 12597942 4 20160119 20160123 0
125979421 12597942 5 20160119 0