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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5902699 | 6774899 | I | 5902699-7 | 20071215 | 20080916 | 20080930 | EXP | DK-RANBAXY-2008RR-18292 | RANBAXYUS | M | Y | 108 | KG | 20080930 | OT | DENMARK |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
5902699 | 1010518144 | PS | SIMVASTATIN RANBAXY FILM COATED TABLETS 10MG | 2 | ORAL | 10 MG, UNK | 76285 | ||||
5902699 | 1010518145 | C | CENTYL | 2 | ORAL | UNK |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5902699 | 1010518144 | HYPERCHOLESTEROLAEMIA |
5902699 | 1010518145 | DIURETIC THERAPY |
Outcome of event
Event ID | OUTC COD |
---|---|
5902699 | DS |
Reactions reported
Event ID | PT |
---|---|
5902699 | INTERSTITIAL LUNG DISEASE |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5902699 | 1010518144 | 20050715 | 20080707 | 1089 | DAY |