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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125607402 | 12560740 | 2 | F | 20160406 | 20160711 | 20160715 | 20160725 | EXP | DE-SUN PHARMACEUTICAL INDUSTRIES LTD-2016R1-120058 | RANBAXY | 73.00 | YR | F | Y | 0.00000 | 20160725 | OT | DE | DE |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125607402 | 12560740 | 1 | PS | ALLOPURINOL. | ALLOPURINOL | 1 | Oral | UNK | Y | U | 78390 | ||||||||
| 125607402 | 12560740 | 2 | C | MARCUMAR | PHENPROCOUMON | 1 | Oral | AFTER INR | U | 0 | |||||||||
| 125607402 | 12560740 | 3 | C | Furosemid | FUROSEMIDE | 1 | Oral | UNK | U | 0 | |||||||||
| 125607402 | 12560740 | 4 | C | METOPROLOL. | METOPROLOL | 1 | Oral | UNK | U | 0 | |||||||||
| 125607402 | 12560740 | 5 | C | RAMIPRIL. | RAMIPRIL | 1 | Oral | UNK | U | 0 | |||||||||
| 125607402 | 12560740 | 6 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Oral | UNK | U | 0 | |||||||||
| 125607402 | 12560740 | 7 | C | Insuline | INSULIN NOS | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125607402 | 12560740 | 1 | Gout |
| 125607402 | 12560740 | 2 | Deep vein thrombosis |
| 125607402 | 12560740 | 3 | Cardiac failure |
| 125607402 | 12560740 | 4 | Hypertension |
| 125607402 | 12560740 | 5 | Product used for unknown indication |
| 125607402 | 12560740 | 6 | Hyperlipidaemia |
| 125607402 | 12560740 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125607402 | 12560740 | OT |
| 125607402 | 12560740 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125607402 | 12560740 | Blood blister | |
| 125607402 | 12560740 | Petechiae | |
| 125607402 | 12560740 | Skin exfoliation | |
| 125607402 | 12560740 | Toxic epidermal necrolysis |
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 |
|---|---|---|---|---|---|---|
| 125607402 | 12560740 | 1 | 20160401 | 20160408 | 0 |