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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116637343 | 11663734 | 3 | F | 20160624 | 20151027 | 20160706 | EXP | US-ASTELLAS-2015US039070 | ASTELLAS | 71.00 | YR | F | Y | 0.00000 | 20160706 | OT | GB | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116637343 | 11663734 | 1 | PS | TACROLIMUS. | TACROLIMUS | 1 | Unknown | U | 50708 | 3 | MG | FORMULATION UNKNOWN | BID | ||||||
| 116637343 | 11663734 | 2 | I | DABIGATRAN | DABIGATRAN | 1 | Unknown | Y | 0 | 150 | MG | FORMULATION UNKNOWN | BID | ||||||
| 116637343 | 11663734 | 3 | C | HYDROXYCHLOROQUINE | HYDROXYCHLOROQUINE | 1 | Unknown | U | 0 | 200 | MG | FORMULATION UNKNOWN | QD | ||||||
| 116637343 | 11663734 | 4 | C | PROPAFENONE. | PROPAFENONE | 1 | Unknown | U | 0 | 225 | MG | FORMULATION UNKNOWN | BID | ||||||
| 116637343 | 11663734 | 5 | C | VALSARTAN. | VALSARTAN | 1 | Unknown | U | 0 | 80 | MG | FORMULATION UNKNOWN | QD | ||||||
| 116637343 | 11663734 | 6 | C | RANITIDINE. | RANITIDINE | 1 | Unknown | U | 0 | 150 | MG | FORMULATION UNKNOWN | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116637343 | 11663734 | 1 | Liver transplant |
| 116637343 | 11663734 | 2 | Atrial fibrillation |
| 116637343 | 11663734 | 3 | Rheumatoid arthritis |
| 116637343 | 11663734 | 4 | Atrial fibrillation |
| 116637343 | 11663734 | 5 | Hypertension |
| 116637343 | 11663734 | 6 | Gastrooesophageal reflux disease |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 116637343 | 11663734 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116637343 | 11663734 | Conjunctival haemorrhage | |
| 116637343 | 11663734 | Drug interaction | |
| 116637343 | 11663734 | International normalised ratio increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |