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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127087471 | 12708747 | 1 | I | 20160726 | 20160805 | 20160901 | 20160901 | PER | US-GILEAD-2016-0227099 | GILEAD | 62.00 | YR | A | M | Y | 86.40000 | KG | 20160901 | PH | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127087471 | 12708747 | 1 | PS | HARVONI | LEDIPASVIRSOFOSBUVIR | 1 | Oral | 1 DF, UNK | Y | 205834 | 1 | DF | TABLET | ||||||
| 127087471 | 12708747 | 2 | SS | AMIODARONE | AMIODARONE | 1 | Intravenous (not otherwise specified) | 0.5 MG, UNK | U | 0 | .5 | MG | |||||||
| 127087471 | 12708747 | 3 | C | BUSULFAN. | BUSULFAN | 1 | UNK | 0 | |||||||||||
| 127087471 | 12708747 | 4 | C | CYTOXAN | CYCLOPHOSPHAMIDE | 1 | UNK | 0 | |||||||||||
| 127087471 | 12708747 | 5 | C | DEXAMETHASONE. | DEXAMETHASONE | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 6 | C | DOCUSATE SODIUM. | DOCUSATE SODIUM | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 7 | C | FILGRASTIM | FILGRASTIM | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 8 | C | CHOLECALCIFEROL | CHOLECALCIFEROL | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 9 | C | HEPARIN | HEPARIN SODIUM | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 10 | C | INSULIN ASPART | INSULIN ASPART | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 11 | C | MULTIVITAMIN /00097801/ | VITAMINS | 1 | 0 | ||||||||||||
| 127087471 | 12708747 | 12 | C | VALACYCLOVIR | VALACYCLOVIR HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127087471 | 12708747 | 1 | Hepatitis C |
| 127087471 | 12708747 | 2 | Atrial fibrillation |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127087471 | 12708747 | LT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127087471 | 12708747 | Bradycardia |
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 |
|---|---|---|---|---|---|---|
| 127087471 | 12708747 | 1 | 20160523 | 20160726 | 0 | |
| 127087471 | 12708747 | 2 | 20160724 | 20160726 | 0 | |
| 127087471 | 12708747 | 3 | 20160718 | 0 | ||
| 127087471 | 12708747 | 4 | 20160718 | 0 |