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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126436341 | 12643634 | 1 | I | 20160804 | 20160811 | 20160811 | EXP | CA-AMGEN-CANSP2016101833 | AMGEN | 65.00 | YR | E | M | Y | 89.00000 | KG | 20160811 | OT | CA | CA |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126436341 | 12643634 | 1 | PS | PROLIA | DENOSUMAB | 1 | Subcutaneous | UNK | U | 125320 | SOLUTION FOR INJECTION | ||||||||
| 126436341 | 12643634 | 2 | SS | CLAVULIN | AMOXICILLINCLAVULANIC ACID | 1 | Unknown | UNK | 0 | ||||||||||
| 126436341 | 12643634 | 3 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 900 MG, Q2WK | 0 | 900 | MG | QOW | |||||||
| 126436341 | 12643634 | 4 | SS | SOLIRIS | ECULIZUMAB | 1 | Intravenous (not otherwise specified) | 600 MG, QWK | 0 | 600 | MG | /wk | |||||||
| 126436341 | 12643634 | 5 | C | ACETAMINOPHEN. | ACETAMINOPHEN | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 6 | C | ACETYLSALICYLIC ACID | ASPIRIN | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 7 | C | ACTONEL | RISEDRONATE SODIUM | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 8 | C | ALPHAGAN P | BRIMONIDINE TARTRATE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 9 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 10 | C | ATACAND | CANDESARTAN CILEXETIL | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 11 | C | AZOPT | BRINZOLAMIDE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 12 | C | CORTISONE | CORTISONEHYDROCORTISONE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 13 | C | FERROUS SULFATE. | FERROUS SULFATE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 14 | C | GLUCONORM | REPAGLINIDE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 15 | C | GLUCOPHAGE | METFORMIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 16 | C | LASIX | FUROSEMIDE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 17 | C | LOSEC | OMEPRAZOLE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 18 | C | MAGNESIUM | MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 19 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 20 | C | NAPROXEN. | NAPROXEN | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 21 | C | NORVASC | AMLODIPINE BESYLATE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 22 | C | NOVOLIN GE TORONTO | INSULIN HUMAN | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 23 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 24 | C | PREDNISONE. | PREDNISONE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 25 | C | PREDNISOLONE. | PREDNISOLONE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 26 | C | STATEX | MORPHINE SULFATE | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 27 | C | TYLENOL ARTHRITIS PAIN | ACETAMINOPHEN | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 28 | C | VITAMIN B12 | CYANOCOBALAMIN | 1 | UNK | 0 | |||||||||||
| 126436341 | 12643634 | 29 | C | VOLTAREN | DICLOFENAC SODIUM | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126436341 | 12643634 | 1 | Product used for unknown indication |
| 126436341 | 12643634 | 2 | Product used for unknown indication |
| 126436341 | 12643634 | 3 | Paroxysmal nocturnal haemoglobinuria |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126436341 | 12643634 | HO |
| 126436341 | 12643634 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126436341 | 12643634 | Abdominal pain upper | |
| 126436341 | 12643634 | Asthenia | |
| 126436341 | 12643634 | Blood magnesium decreased | |
| 126436341 | 12643634 | Diarrhoea | |
| 126436341 | 12643634 | Haemoglobin decreased | |
| 126436341 | 12643634 | Haemorrhage urinary tract | |
| 126436341 | 12643634 | Hypophagia | |
| 126436341 | 12643634 | Jaundice | |
| 126436341 | 12643634 | Mental status changes | |
| 126436341 | 12643634 | Pain in extremity | |
| 126436341 | 12643634 | Pyrexia | |
| 126436341 | 12643634 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |