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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124568012 | 12456801 | 2 | F | 20160412 | 20160721 | 20160610 | 20160802 | EXP | FR-FRI-1000085207 | FOREST | 77.19 | YR | F | Y | 0.00000 | 20160802 | OT | DK | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124568012 | 12456801 | 1 | PS | ESCITALOPRAM | ESCITALOPRAM OXALATE | 1 | Oral | 5 MG | Y | 21323 | 5 | MG | QD | ||||||
| 124568012 | 12456801 | 2 | SS | PACLITAXEL HOSPIRA | PACLITAXEL | 1 | Intravenous (not otherwise specified) | 60 MG/M2 | 0 | ||||||||||
| 124568012 | 12456801 | 3 | SS | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | 1 DF | Y | 0 | 1 | DF | QD | ||||||
| 124568012 | 12456801 | 4 | SS | TELMISARTAN. | TELMISARTAN | 1 | Oral | 1 DF | Y | 0 | 1 | DF | QD | ||||||
| 124568012 | 12456801 | 5 | SS | HEPT A MYL | HEPTAMINOL HYDROCHLORIDE | 1 | Oral | 3 DF | Y | 0 | 3 | DF | TABLET | QD | |||||
| 124568012 | 12456801 | 6 | C | ZOPICLONE | ZOPICLONE | 1 | 0 | ||||||||||||
| 124568012 | 12456801 | 7 | C | PARACETAMOL | ACETAMINOPHEN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124568012 | 12456801 | 1 | Product used for unknown indication |
| 124568012 | 12456801 | 2 | Osteitis deformans |
| 124568012 | 12456801 | 3 | Product used for unknown indication |
| 124568012 | 12456801 | 4 | Product used for unknown indication |
| 124568012 | 12456801 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 124568012 | 12456801 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124568012 | 12456801 | Acute prerenal failure | |
| 124568012 | 12456801 | Dehydration | |
| 124568012 | 12456801 | Diarrhoea | |
| 124568012 | 12456801 | Fatigue | |
| 124568012 | 12456801 | Hyponatraemia | |
| 124568012 | 12456801 | Renal failure | |
| 124568012 | 12456801 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 124568012 | 12456801 | 1 | 20160418 | 0 | ||
| 124568012 | 12456801 | 2 | 20160322 | 20160322 | 0 | |
| 124568012 | 12456801 | 3 | 20160418 | 0 | ||
| 124568012 | 12456801 | 4 | 20160418 | 0 | ||
| 124568012 | 12456801 | 5 | 20160418 | 0 |