The Safety Rates Drug Report

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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
4466791 5665033 I 4466791-9 20010101 20040922 20040930 EXP TPA2004A01147 TAKEDA PHARMACEUTICALS NORTH AMERICA. 53 YR F N 20040929 CN

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
4466791 1005268383 PS ACTOS 1 ORAL 30 MG, 1 IN 1 D, PER ORAL (SEE IMAGE) D D 21073
4466791 1005290621 SS AMARYL 1 ORAL 2 MG, 1 IN 1 D; PER ORAL
4466791 1005290622 SS GLUCOPHAGE 1 ORAL 850 MG, 2 IN 1 D; PER ORAL
4466791 1005290624 C ACCUPRIL (QUINAPRIL HYDROCHLORIDE) (40 MILLIGRAM) 2
4466791 1005290625 C NORVASC (AMLODIPINE) (5 MILLIGRAM) 2
4466791 1005290628 C HCTZ (HYDROCHLOROTHIAZIDE) (12.5 MILLIGRAM) 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
4466791 1005268383 DIABETES MELLITUS NON-INSULIN-DEPENDENT
4466791 1005290621 DIABETES MELLITUS NON-INSULIN-DEPENDENT
4466791 1005290622 DIABETES MELLITUS NON-INSULIN-DEPENDENT

Outcome of event

Event ID OUTC COD
4466791 DS
4466791 RI

Reactions reported

Event ID PT
4466791 BLINDNESS
4466791 BLOOD GLUCOSE DECREASED
4466791 DIZZINESS
4466791 EYELID BLEEDING
4466791 HAEMORRHAGE
4466791 TREMOR

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

Event ID RPSR COD
4466791 CSM

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
4466791 1005268383 20040722