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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123686475 | 12368647 | 5 | F | 20160706 | 20160513 | 20160712 | EXP | US-009507513-1605USA002448 | MERCK | 8.00 | YR | F | Y | 0.00000 | 20160709 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123686475 | 12368647 | 1 | PS | FUROSEMIDE. | FUROSEMIDE | 1 | Oral | UNK | U | 70017 | TABLET | ||||||||
| 123686475 | 12368647 | 2 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | U | 70017 | TABLET | ||||||||||
| 123686475 | 12368647 | 3 | SS | PROPRANOLOL HYDROCHLORIDE. | PROPRANOLOL HYDROCHLORIDE | 1 | UNK | U | 0 | ||||||||||
| 123686475 | 12368647 | 4 | SS | BEVACIZUMAB | BEVACIZUMAB | 1 | UNK | U | 0 | ||||||||||
| 123686475 | 12368647 | 5 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | U | 0 | |||||||||||
| 123686475 | 12368647 | 6 | SS | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123686475 | 12368647 | 1 | Portal hypertension |
| 123686475 | 12368647 | 2 | Ascites |
| 123686475 | 12368647 | 3 | Cutaneovisceral angiomatosis with thrombocytopenia |
| 123686475 | 12368647 | 4 | Cutaneovisceral angiomatosis with thrombocytopenia |
| 123686475 | 12368647 | 5 | Portal hypertension |
| 123686475 | 12368647 | 6 | Ascites |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123686475 | 12368647 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123686475 | 12368647 | Ascites | |
| 123686475 | 12368647 | Drug ineffective | |
| 123686475 | 12368647 | Dyspnoea | |
| 123686475 | 12368647 | Epistaxis | |
| 123686475 | 12368647 | Haematemesis | |
| 123686475 | 12368647 | Hepatic failure | |
| 123686475 | 12368647 | Thrombocytopenia |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |