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
4745063 6026923 I 4745063-9 20050703 20050801 20050812 EXP 2005110225 PFIZER INC 80 YR F N 20050811 OT UNITED KINGDOM

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
4745063 1006319651 PS DOXAZOSIN 2 ORAL 4 MG (4 MG, DAILY),ORAL Y D 19668
4745063 1006343710 SS AMITRIPTYLINE HYDROCHLORIDE 1 ORAL 10 MG (10 MG, DAILY),ORAL Y D
4745063 1006343712 SS FURSEMIDE 2 80 MG (80 MG, DAILY) Y D
4745063 1006343713 SS GLICLAZIDE 2 80 MG (80 MG, DAILY) Y D
4745063 1006343714 SS ETODOLAC 1 600 MG (300 MG, BID) Y D
4745063 1006343716 C ASPIRIN 1
4745063 1006343717 C FERROUS SULFATE TAB 1
4745063 1006343719 C HUMAN MIXTARD (INSULIN HUMAN, INSULIN HUMAN INJECTION, ISOPHANE) 2
4745063 1006343720 C BETNOVATE (BETAMETHASONE) 2
4745063 1006343721 C EUMOVATE (CLOBETASONE BUTYRATE) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4745063 1006319651 ILL-DEFINED DISORDER
4745063 1006343710 ILL-DEFINED DISORDER
4745063 1006343712 ILL-DEFINED DISORDER
4745063 1006343713 ILL-DEFINED DISORDER
4745063 1006343714 ILL-DEFINED DISORDER

Outcome of event

Event ID OUTC COD
4745063 HO

Reactions reported

Event ID PT
4745063 DERMATITIS EXFOLIATIVE

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

Event ID RPSR COD
4745063 FGN
4745063 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4745063 1006319651 20050704
4745063 1006343710 20050704
4745063 1006343712 20050704
4745063 1006343713 20050704
4745063 1006343714 20050704