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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125226872 | 12522687 | 2 | F | 201601 | 20160701 | 20160701 | 20160706 | EXP | AT-GILEAD-2016-0221595 | GILEAD | 87.00 | YR | E | F | Y | 0.00000 | 20160706 | MD | AT | AT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125226872 | 12522687 | 1 | PS | RANOLAZINE | RANOLAZINE | 1 | Unknown | 375 MG, QD | N | 21526 | 375 | MG | TABLET | QD | |||||
| 125226872 | 12522687 | 2 | SS | RANOLAZINE | RANOLAZINE | 1 | Unknown | 750 MG, QD | N | 21526 | 750 | MG | TABLET | QD | |||||
| 125226872 | 12522687 | 3 | SS | MIRTAZAPINE. | MIRTAZAPINE | 1 | Unknown | UNK | U | U | 0 | ||||||||
| 125226872 | 12522687 | 4 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | 80 MG, QD | U | 0 | 80 | MG | QD | ||||||
| 125226872 | 12522687 | 5 | C | PHENPROCOUMON | PHENPROCOUMON | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 6 | C | CARVEDILOL. | CARVEDILOL | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 7 | C | LISINOPRIL. | LISINOPRIL | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 8 | C | NICORANDIL | NICORANDIL | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 9 | C | GLYCERYL TRINITRATE | NITROGLYCERIN | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 10 | C | PANTOPRAZOLE SODIUM SESQUIHYDRATE | PANTOPRAZOLE SODIUM | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 11 | C | QUETIAPINE FUMARATE. | QUETIAPINE FUMARATE | 1 | 0 | ||||||||||||
| 125226872 | 12522687 | 12 | C | FENTANYL. | FENTANYL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125226872 | 12522687 | 1 | Angina pectoris |
| 125226872 | 12522687 | 3 | Pain |
| 125226872 | 12522687 | 4 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125226872 | 12522687 | HO |
| 125226872 | 12522687 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125226872 | 12522687 | Hyponatraemia | |
| 125226872 | 12522687 | Intentional underdose | |
| 125226872 | 12522687 | Nausea | |
| 125226872 | 12522687 | Off label use | |
| 125226872 | 12522687 | 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 |
|---|---|---|---|---|---|---|
| 125226872 | 12522687 | 2 | 2015 | 0 |