The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
6918934 7495312 F 6918934-2 20090101 20100809 20100811 EXP IT-BRISTOL-MYERS SQUIBB COMPANY-15199797 BRISTOL-MYERS SQUIBB COMPANY 78 YR F Y 20100811 MD ITALY

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
6918934 1014391923 PS COUMADIN 1 ORAL 009218
6918934 1014391924 I FENOFIBRATE 1 ORAL
6918934 1014391925 C DILTIAZEM HCL 1 ORAL 200 MG LONG RELEASE CAPS
6918934 1014391926 C NEO-LOTAN 2 ORAL 50 MG TABS
6918934 1014391927 C TORADIUR 2 ORAL 10 MG TABS
6918934 1014391928 C EUTIROX 2 ORAL 25 MCG TABS

Indications of drugs used

Event ID DRUG SEQ INDI PT
6918934 1014391923 THROMBOSIS PROPHYLAXIS
6918934 1014391924 DYSLIPIDAEMIA
6918934 1014391925 HYPERTENSION
6918934 1014391926 HYPERTENSION
6918934 1014391927 HYPERTENSION
6918934 1014391928 HYPOTHYROIDISM

Outcome of event

Event ID OUTC COD
6918934 HO
6918934 OT

Reactions reported

Event ID PT
6918934 ANAEMIA
6918934 DRUG INTERACTION
6918934 HAEMATOCHEZIA
6918934 INTERNATIONAL NORMALISED RATIO INCREASED
6918934 MELAENA
6918934 RENAL IMPAIRMENT
6918934 SUBCUTANEOUS HAEMATOMA

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6918934 1014391923 20080401 20090630
6918934 1014391925 20100401