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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125796523 | 12579652 | 3 | F | 201607 | 20160725 | 20160721 | 20160804 | EXP | US-ELI_LILLY_AND_COMPANY-US201607005687 | ELI LILLY AND CO | 65.76 | YR | F | Y | 97.05000 | KG | 20160804 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125796523 | 12579652 | 1 | PS | ADCIRCA | TADALAFIL | 1 | Unknown | UNK, UNKNOWN | 21368 | TABLET | |||||||||
| 125796523 | 12579652 | 2 | SS | LETAIRIS | AMBRISENTAN | 1 | Unknown | UNK, UNKNOWN | U | 1413104A | 0 | 5 | MG | QD | |||||
| 125796523 | 12579652 | 3 | SS | REMODULIN | TREPROSTINIL | 1 | Intravenous (not otherwise specified) | 43 NG/KG/MIN CONTINUOUS | U | 2100909 | 0 | ||||||||
| 125796523 | 12579652 | 4 | C | WARFARIN | WARFARIN | 1 | Unknown | UNK, UNKNOWN | 0 | ||||||||||
| 125796523 | 12579652 | 5 | C | DILTIAZEM. | DILTIAZEM | 1 | Unknown | UNK UNK, UNKNOWN | 0 | ||||||||||
| 125796523 | 12579652 | 6 | C | OFEV | NINTEDANIB | 1 | Unknown | UNK, UNKNOWN | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125796523 | 12579652 | 1 | Pulmonary arterial hypertension |
| 125796523 | 12579652 | 2 | Pulmonary arterial hypertension |
| 125796523 | 12579652 | 3 | Pulmonary arterial hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125796523 | 12579652 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125796523 | 12579652 | Headache | |
| 125796523 | 12579652 | Nausea | |
| 125796523 | 12579652 | Oedema | |
| 125796523 | 12579652 | Vomiting | |
| 125796523 | 12579652 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 125796523 | 12579652 | 2 | 20160713 | 0 | ||
| 125796523 | 12579652 | 3 | 20151118 | 20160713 | 0 |