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
4624197 5768582 I 4624197-3 20010710 20050322 20050331 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-12911913 BRISTOL-MYERS SQUIBB COMPANY 69 YR F Y 20050331 OT

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
4624197 1005835820 PS APROVEL TABS 150 MG 2 ORAL 20757
4624197 1005835821 SS ALDACTONE 1
4624197 1005835822 SS DIGOXINE NATIVELLE 2
4624197 1005835823 C LASILIX 2
4624197 1005835824 C METFORMIN HCL 1 021202

Indications of drugs used

Event ID DRUG SEQ INDI PT
4624197 1005835820 CARDIAC FAILURE
4624197 1005835821 CARDIAC FAILURE

Outcome of event

Event ID OUTC COD
4624197 HO
4624197 LT
4624197 OT

Reactions reported

Event ID PT
4624197 ATRIOVENTRICULAR BLOCK COMPLETE
4624197 BRADYCARDIA
4624197 HYPERKALAEMIA
4624197 HYPONATRAEMIA
4624197 OVERDOSE
4624197 RENAL FAILURE ACUTE

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
4624197 1005835820 20010711
4624197 1005835821 19990604 20010710
4624197 1005835822 20010710
4624197 1005835823 20010710
4624197 1005835824 20010710