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
4738397 5834619 F 4738397-5 20050324 20050704 20050809 EXP FR-GLAXOSMITHKLINE-B0387006A GLAXOSMITHKLINE 57 YR M Y 120 KG 20050809 CN 20050604 FRANCE

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
4738397 1006296847 PS AUGMENTIN '125' 1 UNKNOWN 50564
4738397 1006296848 SS FLAGYL 1 UNKNOWN
4738397 1006296849 SS CARDENSIEL 2 UNKNOWN
4738397 1006296850 SS PREVISCAN 20 2 ORAL
4738397 1006296851 C MONICOR LP 2 UNKNOWN
4738397 1006296852 C ZESTRIL 1 UNKNOWN
4738397 1006296853 C PLAVIX 1 UNKNOWN
4738397 1006296854 C LASIX 1 UNKNOWN
4738397 1006296855 C CORDARONE 1 UNKNOWN

Indications of drugs used

Event ID DRUG SEQ INDI PT
4738397 1006296847 SKIN ULCER
4738397 1006296848 SKIN ULCER

Outcome of event

Event ID OUTC COD
4738397 DE
4738397 HO

Reactions reported

Event ID PT
4738397 DERMATITIS BULLOUS
4738397 LEG AMPUTATION
4738397 LEUKOCYTOCLASTIC VASCULITIS
4738397 PURPURA
4738397 RASH PRURITIC
4738397 SEPSIS
4738397 SEPTIC SHOCK

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
4738397 1006296847 20050320 20050323 4 DAY
4738397 1006296848 20050320 20050323 4 DAY
4738397 1006296850 20050324