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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126581821 | 12658182 | 1 | I | 20160812 | 20160817 | 20160817 | EXP | AU-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00363 | SCIEGEN | 53.00 | YR | M | Y | 0.00000 | 20160817 | CN | AU | AU |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126581821 | 12658182 | 1 | PS | ATORVASTATIN CALCIUM. | ATORVASTATIN CALCIUM | 1 | Unknown | 7X40MG (280MG) | U | U | 205519 | 40 | MG | TABLET | |||||
| 126581821 | 12658182 | 2 | SS | Apixaban | APIXABAN | 1 | Unknown | 40X5MG (200MG) | U | U | 0 | 5 | MG | ||||||
| 126581821 | 12658182 | 3 | SS | RAMIPRIL. | RAMIPRIL | 1 | Unknown | 28X1.25MG (35MG) | U | U | 0 | 1.25 | MG | ||||||
| 126581821 | 12658182 | 4 | SS | Bisoprolol | BISOPROLOL | 1 | Unknown | 42 X 2.5MG (105MG) | U | U | 0 | 2.5 | MG | ||||||
| 126581821 | 12658182 | 5 | SS | COLCHICINE. | COLCHICINE | 1 | Unknown | 12 X 0.5MG (6MG) | U | U | 0 | .5 | MG | ||||||
| 126581821 | 12658182 | 6 | SS | Magnesium | MAGNESIUM | 1 | Unknown | 10 X 3.74MG (37.4MG) | U | U | 0 | 3.74 | MG | ||||||
| 126581821 | 12658182 | 7 | SS | Paracetmol | ACETAMINOPHEN | 1 | Unknown | 4 X 500MG | U | 0 | 500 | MG | |||||||
| 126581821 | 12658182 | 8 | SS | Codeine | CODEINE | 1 | Unknown | 9.5 MG, UNK | U | U | 0 | 9.5 | MG | ||||||
| 126581821 | 12658182 | 9 | SS | PHENYLEPHRINE | PHENYLEPHRINEPHENYLEPHRINE HYDROCHLORIDE | 1 | Unknown | 5 MG, UNK | U | U | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126581821 | 12658182 | 1 | Product used for unknown indication |
| 126581821 | 12658182 | 2 | Atrial fibrillation |
| 126581821 | 12658182 | 3 | Product used for unknown indication |
| 126581821 | 12658182 | 4 | Product used for unknown indication |
| 126581821 | 12658182 | 5 | Product used for unknown indication |
| 126581821 | 12658182 | 6 | Product used for unknown indication |
| 126581821 | 12658182 | 7 | Product used for unknown indication |
| 126581821 | 12658182 | 8 | Product used for unknown indication |
| 126581821 | 12658182 | 9 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126581821 | 12658182 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126581821 | 12658182 | Activated partial thromboplastin time prolonged | |
| 126581821 | 12658182 | Hypotension | |
| 126581821 | 12658182 | International normalised ratio increased | |
| 126581821 | 12658182 | Overdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |