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
6729702 7395040 I 6729702-9 20091216 20100505 20100512 EXP TPA2010A02642 TAKEDA PHARMACEUTICALS NORTH AMERICA. 62 YR M N 98.7 KG 20100511 MD UNITED STATES

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
6729702 1013705162 PS ACTOS 1 ORAL 15 MG, 1 IN 1 D, PER ORAL Y D 21073
6729702 1013724835 SS LANTUS 1 SUBCUTANEOUS 16 IU, 1 IN 1 D, SUBCUTANEOUS
6729702 1013724837 SS GLIPIZIDE 1 ORAL 10 MG, 2 IN 1 D, PER ORAL
6729702 1013724850 SS HPN-100 (INVESTIGATIONAL DRUG) 2
6729702 1013724852 C PRAVACHOL 1
6729702 1013724858 C SPIRONOLACTONE 1
6729702 1013724860 C FUROSEMIDE 1
6729702 1013724862 C OMEPRAZOLE MAGNESIUM (OMEPRAZOLE MAGNESIUM) 2
6729702 1013724864 C HALDOL 1
6729702 1013724865 C MEN'S MULTIVITAMIN (ERGOCALCIFEROL, ASCORBIC ACID, FOLIC ACID, THIAMIN 2
6729702 1013724867 C ASPIRIN 1
6729702 1013724868 C LACTULOSE 1

Indications of drugs used

Event ID DRUG SEQ INDI PT
6729702 1013705162 TYPE 2 DIABETES MELLITUS
6729702 1013724835 TYPE 2 DIABETES MELLITUS
6729702 1013724837 TYPE 2 DIABETES MELLITUS
6729702 1013724850 HEPATIC ENCEPHALOPATHY

Outcome of event

Event ID OUTC COD
6729702 HO

Reactions reported

Event ID PT
6729702 HYPOGLYCAEMIA
6729702 LOSS OF CONSCIOUSNESS
6729702 POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME

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

Event ID RPSR COD
6729702 HP
6729702 SDY

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6729702 1013705162 20080917 20091216
6729702 1013724837 20090504 20091216
6729702 1013724850 20091201