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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281333 | 12528133 | 3 | F | 2000 | 20160921 | 20160705 | 20160928 | EXP | US-PFIZER INC-2016322941 | PFIZER | 71.00 | YR | F | Y | 47.17000 | KG | 20160928 | MD | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125281333 | 12528133 | 1 | PS | SIROLIMUS. | SIROLIMUS | 1 | Oral | 2 MG, DAILY (2 MG, 1 TABLET A DAY BY MOUTH) | 21110 | 2 | MG | TABLET | |||||||
| 125281333 | 12528133 | 2 | SS | SIROLIMUS. | SIROLIMUS | 1 | 21110 | TABLET | |||||||||||
| 125281333 | 12528133 | 3 | C | PREVACID | LANSOPRAZOLE | 1 | Oral | (1 DF, 1X/DAY) 30 MG, 1X/DAY | 0 | 30 | MG | QD | |||||||
| 125281333 | 12528133 | 4 | C | PREVACID | LANSOPRAZOLE | 1 | 0 | ||||||||||||
| 125281333 | 12528133 | 5 | C | METOPROLOL TARTRATE. | METOPROLOL TARTRATE | 1 | Oral | 25 MG, 2X/DAY | 0 | 25 | MG | BID | |||||||
| 125281333 | 12528133 | 6 | C | PREDNISONE. | PREDNISONE | 1 | Oral | 5 MG, 1X/DAY | 0 | 5 | MG | TABLET | QD | ||||||
| 125281333 | 12528133 | 7 | C | EFFEXOR XR | VENLAFAXINE HYDROCHLORIDE | 1 | Oral | 75 MG, 1X/DAY | 0 | 75 | MG | TABLET | QD | ||||||
| 125281333 | 12528133 | 8 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | Oral | 25 MG, 1X/DAY | 0 | 25 | MG | TABLET | QD | ||||||
| 125281333 | 12528133 | 9 | C | VENLAFAXINE | VENLAFAXINE HYDROCHLORIDE | 1 | 75 MG, 1X/DAY | 0 | 75 | MG | QD | ||||||||
| 125281333 | 12528133 | 10 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | 1000 IU, 1X/DAY | 0 | 1000 | IU | QD | ||||||||
| 125281333 | 12528133 | 11 | C | TURMERIC | TURMERIC | 1 | UNK, 1X/DAY | 0 | QD | ||||||||||
| 125281333 | 12528133 | 12 | C | POTASSIUM GLUCONATE | POTASSIUM GLUCONATE | 1 | 595 MG, 1X/DAY | 0 | 595 | MG | QD | ||||||||
| 125281333 | 12528133 | 13 | C | CALCIUM | CALCIUM | 1 | 600 MG, 1X/DAY | 0 | 600 | MG | QD | ||||||||
| 125281333 | 12528133 | 14 | C | FIBERCON | CALCIUM POLYCARBOPHIL | 1 | 2 DF, 1X/DAY | 0 | 2 | DF | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125281333 | 12528133 | 1 | Prophylaxis against transplant rejection |
| 125281333 | 12528133 | 2 | Liver transplant |
| 125281333 | 12528133 | 3 | Oesophageal disorder |
| 125281333 | 12528133 | 4 | Oesophageal ulcer |
| 125281333 | 12528133 | 5 | Hypertension |
| 125281333 | 12528133 | 6 | Infection prophylaxis |
| 125281333 | 12528133 | 7 | Depression |
| 125281333 | 12528133 | 8 | Peripheral swelling |
| 125281333 | 12528133 | 9 | Jaw disorder |
| 125281333 | 12528133 | 10 | Supplementation therapy |
| 125281333 | 12528133 | 11 | Pain |
| 125281333 | 12528133 | 12 | Blood potassium decreased |
| 125281333 | 12528133 | 13 | Blood calcium decreased |
| 125281333 | 12528133 | 14 | Diarrhoea |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125281333 | 12528133 | HO |
| 125281333 | 12528133 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125281333 | 12528133 | Biliary cirrhosis primary | |
| 125281333 | 12528133 | Depression | |
| 125281333 | 12528133 | Dizziness | |
| 125281333 | 12528133 | Drug ineffective for unapproved indication | |
| 125281333 | 12528133 | Fall | |
| 125281333 | 12528133 | Fatigue | |
| 125281333 | 12528133 | Humerus fracture | |
| 125281333 | 12528133 | Intentional underdose | |
| 125281333 | 12528133 | Lethargy | |
| 125281333 | 12528133 | Liver transplant rejection | |
| 125281333 | 12528133 | Nausea | |
| 125281333 | 12528133 | 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 |
|---|---|---|---|---|---|---|
| 125281333 | 12528133 | 1 | 2000 | 0 | ||
| 125281333 | 12528133 | 3 | 2008 | 0 | ||
| 125281333 | 12528133 | 5 | 2011 | 0 | ||
| 125281333 | 12528133 | 6 | 2000 | 0 | ||
| 125281333 | 12528133 | 7 | 2000 | 0 | ||
| 125281333 | 12528133 | 8 | 2011 | 0 | ||
| 125281333 | 12528133 | 10 | 2012 | 0 | ||
| 125281333 | 12528133 | 11 | 2015 | 0 | ||
| 125281333 | 12528133 | 12 | 2013 | 0 | ||
| 125281333 | 12528133 | 13 | 2000 | 0 | ||
| 125281333 | 12528133 | 14 | 2011 | 0 |