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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126106102 | 12610610 | 2 | F | 20160630 | 20160811 | 20160801 | 20160901 | PER | US-ELI_LILLY_AND_COMPANY-US201607008912 | ELI LILLY AND CO | 83.00 | YR | F | Y | 0.00000 | 20160901 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126106102 | 12610610 | 1 | PS | ADCIRCA | TADALAFIL | 1 | Oral | UNK, UNKNOWN | U | U | 21368 | TABLET | |||||||
| 126106102 | 12610610 | 2 | SS | AMBRISENTAN | AMBRISENTAN | 1 | Oral | 5 MG, QD | U | 1413104A | 0 | 5 | MG | TABLET | QD | ||||
| 126106102 | 12610610 | 3 | C | XANAX | ALPRAZOLAM | 1 | 0 | ||||||||||||
| 126106102 | 12610610 | 4 | C | METOPROLOL SUCCINATE. | METOPROLOL SUCCINATE | 1 | 0 | ||||||||||||
| 126106102 | 12610610 | 5 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 0 | ||||||||||||
| 126106102 | 12610610 | 6 | C | ASMANEX | MOMETASONE FUROATE | 1 | 0 | ||||||||||||
| 126106102 | 12610610 | 7 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 0 | ||||||||||||
| 126106102 | 12610610 | 8 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 0 | ||||||||||||
| 126106102 | 12610610 | 9 | C | LOSARTAN. | LOSARTAN | 1 | U | 0 | |||||||||||
| 126106102 | 12610610 | 10 | C | TRAMADOL. | TRAMADOL | 1 | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126106102 | 12610610 | 1 | Product used for unknown indication |
| 126106102 | 12610610 | 2 | Pulmonary hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126106102 | 12610610 | Dyspnoea | |
| 126106102 | 12610610 | Fluid retention | |
| 126106102 | 12610610 | 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 |
|---|---|---|---|---|---|---|
| 126106102 | 12610610 | 2 | 20160621 | 20160630 | 0 |