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 |