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
6669724 7314455 F 6669724-X 20100101 20100318 20100402 EXP THQ2010A00295 TAKEDA PHARMACEUTICALS NORTH AMERICA 61 YR M N 20100401 CZECH REPUBLIC

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
6669724 1013454467 PS ACTOS 1 ORAL 30 MG (30 MG, 1 IN 1 D), PER ORAL D D 21073
6669724 1013530849 C METFORMIN HYDROCHLORIDE 1
6669724 1013530850 C MICARDIS HCT 1
6669724 1013530851 C LEKOPTIN (VERAPAMIL HYDROCHLORIDE) 2
6669724 1013530852 C APO-DICLO /00372302/ (DICLOFENAC SODIUM) 2
6669724 1013530853 C OMEPRAZOLE 1
6669724 1013530854 C SULFASALAZINE 1
6669724 1013530855 C CORTICOSTEROIDS 2

Indications of drugs used

Event ID DRUG SEQ INDI PT
6669724 1013454467 TYPE 2 DIABETES MELLITUS

Outcome of event

Event ID OUTC COD
6669724 HO
6669724 OT

Reactions reported

Event ID PT
6669724 BLOOD CALCIUM DECREASED
6669724 BLOOD OSMOLARITY DECREASED
6669724 BLOOD PRESSURE INCREASED
6669724 BRAIN SCAN ABNORMAL
6669724 ELECTROLYTE DEPLETION
6669724 FALL
6669724 FLUID RETENTION
6669724 HEAD INJURY
6669724 HYPOCHLORAEMIA
6669724 HYPOKALAEMIA
6669724 HYPONATRAEMIA
6669724 INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION
6669724 OSMOTIC DEMYELINATION SYNDROME
6669724 POLYURIA
6669724 SYNCOPE

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

Event ID RPSR COD
6669724 FGN
6669724 HP

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
6669724 1013454467 20090721 20100205 199 DAY