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
6732707 7397110 I 6732707-5 20080223 20100429 20100514 EXP TUK2008A00067 TAKEDA PHARMACEUTICALS NORTH AMERICA. 60 YR F N 20100513 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
6732707 1013716967 PS ACTOS 1 ORAL (45 MG) ORAL Y 21073
6732707 1013736077 SS ROSIGLITAZONE 1 ORAL (8 MG) ORAL
6732707 1013736078 C AMLODIPINE 1
6732707 1013736079 C ASPIRIN 1
6732707 1013736081 C CALCICHEW D3 (COLECALCIFEROL, CALCIUM CARBONATE) 2
6732707 1013736083 C CODEINE PHOSPHATE AND ACETAMINOPHEN 1
6732707 1013736084 C GLICLAZIDE (GLICLAZIDE) 2
6732707 1013736087 C METFORMIN HCL 1
6732707 1013736103 C MODECATE (FLUPHENAZINE DECANOATE) 2
6732707 1013736109 C PROCYCLIDINE HYDROCHLORIDE 2MG TAB 1
6732707 1013736110 C SIMVASTATIN 1
6732707 1013736111 C BENDROFLUAZIDE (BENDROFLUMETHIAZIDE) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6732707 1013716967 DIABETES MELLITUS
6732707 1013736077 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6732707 OT

Reactions reported

Event ID PT
6732707 FALL
6732707 FOOT FRACTURE
6732707 MULTIPLE FRACTURES
6732707 WRIST FRACTURE

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

Event ID RPSR COD
6732707 FGN
6732707 HP
6732707 OTH

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6732707 1013716967 20080109
6732707 1013736077 20070501 20071106