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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112006314 | 11200631 | 4 | F | 20150609 | 20150623 | 20150618 | 20160908 | EXP | TW-UNITED THERAPEUTICS-UNT-2015-007102 | UNITED THERAPEUTICS | 43.36 | YR | F | Y | 0.00000 | 20160908 | CN | ES | TW |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 112006314 | 11200631 | 1 | PS | REMODULIN | TREPROSTINIL | 1 | Subcutaneous | 0.106 ?G/KG/MIN, UNK | U | U | 21272 | .106 | UG/KG | INJECTION | |||||
| 112006314 | 11200631 | 2 | SS | WARFARIN | WARFARIN | 1 | U | U | 0 | ||||||||||
| 112006314 | 11200631 | 3 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 0 | ||||||||||||
| 112006314 | 11200631 | 4 | C | REVATIO | SILDENAFIL CITRATE | 1 | 0 | ||||||||||||
| 112006314 | 11200631 | 5 | C | BOSENTAN. | BOSENTAN | 1 | 0 | ||||||||||||
| 112006314 | 11200631 | 6 | C | CEFADROXIL. | CEFADROXIL | 1 | 0 | ||||||||||||
| 112006314 | 11200631 | 7 | C | RHIN | 2 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 112006314 | 11200631 | 1 | Pulmonary arterial hypertension |
| 112006314 | 11200631 | 2 | Product used for unknown indication |
| 112006314 | 11200631 | 3 | Product used for unknown indication |
| 112006314 | 11200631 | 4 | Product used for unknown indication |
| 112006314 | 11200631 | 5 | Product used for unknown indication |
| 112006314 | 11200631 | 6 | Product used for unknown indication |
| 112006314 | 11200631 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 112006314 | 11200631 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 112006314 | 11200631 | Haematochezia | |
| 112006314 | 11200631 | Haemorrhage |
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 |
|---|---|---|---|---|---|---|
| 112006314 | 11200631 | 1 | 20140502 | 20150609 | 0 |