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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123222892 | 12322289 | 2 | F | 2016 | 20160803 | 20160502 | 20160811 | EXP | NL-ACTELION-A-CH2016-135258 | ACTELION | 87.00 | YR | E | F | Y | 0.00000 | 20160811 | OT | NL | NL |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123222892 | 12322289 | 1 | PS | TRACLEER | BOSENTAN | 1 | Oral | UNK, BID | 21290 | 125 | MG | TABLET | BID | ||||||
| 123222892 | 12322289 | 2 | SS | TRACLEER | BOSENTAN | 1 | Oral | UNK | 21290 | TABLET | |||||||||
| 123222892 | 12322289 | 3 | C | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | 1200 MG, UNK | U | U | 0 | 1200 | MG | |||||||
| 123222892 | 12322289 | 4 | C | CIP | 2 | 500 MG, BID | U | U | 0 | 500 | MG | BID | |||||||
| 123222892 | 12322289 | 5 | C | CALCIUM CARBONATE. | CALCIUM CARBONATE | 1 | UNK | U | U | 0 | |||||||||
| 123222892 | 12322289 | 6 | C | LASIX | FUROSEMIDE | 1 | Intravenous (not otherwise specified) | 40 MG, UNK | U | U | 0 | 40 | MG | ||||||
| 123222892 | 12322289 | 7 | C | CLOPIDOGREL | CLOPIDOGREL BISULFATE | 1 | UNK | U | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123222892 | 12322289 | 1 | Skin ulcer |
| 123222892 | 12322289 | 3 | Product used for unknown indication |
| 123222892 | 12322289 | 4 | Product used for unknown indication |
| 123222892 | 12322289 | 5 | Product used for unknown indication |
| 123222892 | 12322289 | 6 | Product used for unknown indication |
| 123222892 | 12322289 | 7 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123222892 | 12322289 | DE |
| 123222892 | 12322289 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123222892 | 12322289 | Cardiac failure | |
| 123222892 | 12322289 | Fall | |
| 123222892 | 12322289 | Pulmonary sepsis | |
| 123222892 | 12322289 | Renal failure |
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 |
|---|---|---|---|---|---|---|
| 123222892 | 12322289 | 1 | 20071206 | 20160210 | 0 | |
| 123222892 | 12322289 | 2 | 20160410 | 0 | ||
| 123222892 | 12322289 | 3 | 20160202 | 0 | ||
| 123222892 | 12322289 | 5 | 20160202 | 20160330 | 0 | |
| 123222892 | 12322289 | 7 | 20160330 | 0 |