Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116919802 | 11691980 | 2 | F | 20150914 | 20160726 | 20151103 | 20160728 | EXP | DK-DKMA-WBS-0001307 | DK-ROCHE-1654465 | ROCHE | 54.22 | YR | M | Y | 123.00000 | KG | 20160728 | MD | DK | DK |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116919802 | 11691980 | 1 | PS | MABTHERA | RITUXIMAB | 1 | Unknown | SINGLE DOSE | U | 103705 | 1000 | MG | |||||||
116919802 | 11691980 | 2 | SS | PREDNISOLONE ^DAK^ | PREDNISOLONE | 1 | Unknown | U | 0 | 20 | MG | ||||||||
116919802 | 11691980 | 3 | SS | PREDNISOLONE ^DAK^ | PREDNISOLONE | 1 | Unknown | DOSE INCREASED | U | 0 | |||||||||
116919802 | 11691980 | 4 | C | FURIX | FUROSEMIDE | 1 | Oral | 0 | 40 | MG | |||||||||
116919802 | 11691980 | 5 | C | MAREVAN | WARFARIN SODIUM | 1 | Oral | 0 | 2.5 | MG | |||||||||
116919802 | 11691980 | 6 | C | PANTOPRAZOL | PANTOPRAZOLE SODIUM | 1 | Oral | 0 | 40 | MG | |||||||||
116919802 | 11691980 | 7 | C | RAMIPRIL. | RAMIPRIL | 1 | Oral | 0 | 5 | MG | |||||||||
116919802 | 11691980 | 8 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | 0 | 20 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
116919802 | 11691980 | 1 | Nephrotic syndrome |
116919802 | 11691980 | 2 | Nephrotic syndrome |
116919802 | 11691980 | 4 | Diuretic therapy |
116919802 | 11691980 | 5 | Atrial fibrillation |
116919802 | 11691980 | 6 | Prophylaxis against gastrointestinal ulcer |
116919802 | 11691980 | 7 | Product used for unknown indication |
116919802 | 11691980 | 8 | Hypercholesterolaemia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
116919802 | 11691980 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
116919802 | 11691980 | Contusion | |
116919802 | 11691980 | Gait disturbance | |
116919802 | 11691980 | Joint swelling | |
116919802 | 11691980 | Tendon rupture |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | CASEID | DSG DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|---|
116919802 | 11691980 | 1 | 20150910 | 20150910 | 0 | |
116919802 | 11691980 | 2 | 20140212 | 0 |