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
4355529 5710383 I 4355529-1 20040303 20040428 20040510 EXP FR-BRISTOL-MYERS SQUIBB COMPANY-12573176 BRISTOL-MYERS SQUIBB COMPANY 82 YR F Y 20040510 MD

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
4355529 1004849103 PS AMIKLIN INJ 2 INTRAVENOUS
4355529 1004849104 SS CIPROFLOXACIN 1 ORAL
4355529 1004849105 SS VALACYCLOVIR HCL 1 ORAL
4355529 1004849106 SS FLUCONAZOLE 1 ORAL INITIATED AT 50 MG DAILY, INCREASED TO 200 MG DAILY ON 09-MAR-2004
4355529 1004849107 SS PRIMAXIN 1 INTRAVENOUS
4355529 1004849108 C KARDEGIC 2
4355529 1004849109 C LEVOTHYROXINE SODIUM 1
4355529 1004849110 C OMEPRAZOLE 1
4355529 1004849111 C CORDARONE 1
4355529 1004849112 C GARDENAL 2
4355529 1004849113 C ASPEGIC 325 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
4355529 1004849103 SEPSIS
4355529 1004849104 SEPSIS
4355529 1004849105 HERPES ZOSTER
4355529 1004849106 CANDIDIASIS
4355529 1004849107 SEPSIS

Outcome of event

Event ID OUTC COD
4355529 HO
4355529 OT

Reactions reported

Event ID PT
4355529 CANDIDIASIS
4355529 ERYTHEMA
4355529 HERPES ZOSTER
4355529 PRURITUS

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
4355529 1004849103 20040224 20040311 17
4355529 1004849104 20040224 20040311 17
4355529 1004849105 20040303
4355529 1004849106 20040306
4355529 1004849107 20040224 20040311 17
4355529 1004849108 20040308