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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124960702 | 12496070 | 2 | F | 20160513 | 20160714 | 20160624 | 20160718 | PER | US-ELI_LILLY_AND_COMPANY-US201606004501 | ELI LILLY AND CO | 80.00 | YR | F | Y | 0.00000 | 20160718 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 124960702 | 12496070 | 1 | PS | ADCIRCA | TADALAFIL | 1 | Unknown | UNK UNK, UNKNOWN | U | U | 21368 | TABLET | |||||||
| 124960702 | 12496070 | 2 | SS | AMBRISENTAN | AMBRISENTAN | 1 | Unknown | 10 MG, QD | U | 0 | 10 | MG | TABLET | QD | |||||
| 124960702 | 12496070 | 3 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 124960702 | 12496070 | 4 | C | LOSARTAN. | LOSARTAN | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 124960702 | 12496070 | 5 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 124960702 | 12496070 | 6 | C | JANUMET | METFORMIN HYDROCHLORIDESITAGLIPTIN PHOSPHATE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 124960702 | 12496070 | 7 | C | SIMVASTATIN. | SIMVASTATIN | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 124960702 | 12496070 | 8 | C | HYDROCODONE | HYDROCODONE | 1 | Unknown | UNK, UNKNOWN | U | 0 | |||||||||
| 124960702 | 12496070 | 9 | C | IBUPROFEN. | IBUPROFEN | 1 | Unknown | UNK, UNKNOWN | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 124960702 | 12496070 | 1 | Product used for unknown indication |
| 124960702 | 12496070 | 2 | Pulmonary arterial hypertension |
| 124960702 | 12496070 | 3 | Product used for unknown indication |
| 124960702 | 12496070 | 4 | Product used for unknown indication |
| 124960702 | 12496070 | 5 | Product used for unknown indication |
| 124960702 | 12496070 | 6 | Product used for unknown indication |
| 124960702 | 12496070 | 7 | Product used for unknown indication |
| 124960702 | 12496070 | 8 | Product used for unknown indication |
| 124960702 | 12496070 | 9 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 124960702 | 12496070 | Abdominal distension | |
| 124960702 | 12496070 | Dizziness | |
| 124960702 | 12496070 | Dyspnoea | |
| 124960702 | 12496070 | Epistaxis | |
| 124960702 | 12496070 | Fatigue | |
| 124960702 | 12496070 | Paraesthesia | |
| 124960702 | 12496070 | Peripheral swelling |
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 |
|---|---|---|---|---|---|---|
| 124960702 | 12496070 | 2 | 20160509 | 20160622 | 0 |