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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1050079410 | 10500794 | 10 | F | 20140930 | 20160923 | 20141007 | 20160930 | EXP | SE-AMGEN-SWESP2014076354 | AMGEN | 84.00 | YR | E | F | Y | 71.00000 | KG | 20160930 | CN | SE | SE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1050079410 | 10500794 | 1 | PS | PROLIA | DENOSUMAB | 1 | Subcutaneous | 60 MG, Q6MO | 125320 | 60 | MG | SOLUTION FOR INJECTION | |||||||
1050079410 | 10500794 | 2 | C | PANTOPRAZOL | PANTOPRAZOLE SODIUM | 1 | Unknown | 20 MG, QD | 0 | 20 | MG | QD | |||||||
1050079410 | 10500794 | 3 | C | AROMASIN | EXEMESTANE | 1 | Unknown | 25 MG, QD | 0 | 25 | MG | QD | |||||||
1050079410 | 10500794 | 4 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 5 MG, QD | 0 | 5 | MG | QD | |||||||
1050079410 | 10500794 | 5 | C | LOSARTAN AND HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDELOSARTAN POTASSIUM | 1 | Unknown | 100 MG/ 25 MG, QD | 0 | QD | |||||||||
1050079410 | 10500794 | 6 | C | KALCIPOS D3 | 2 | Unknown | 500 MG/400 IE, BID | 0 | BID | ||||||||||
1050079410 | 10500794 | 7 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Unknown | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
1050079410 | 10500794 | 1 | Osteoporosis |
1050079410 | 10500794 | 2 | Prophylaxis |
1050079410 | 10500794 | 3 | Breast cancer |
1050079410 | 10500794 | 4 | Hypertonia |
1050079410 | 10500794 | 5 | Hypertonia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
1050079410 | 10500794 | OT |
1050079410 | 10500794 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
1050079410 | 10500794 | Abdominal pain upper | |
1050079410 | 10500794 | Arthralgia | |
1050079410 | 10500794 | Bacterial test | |
1050079410 | 10500794 | Bursitis infective | |
1050079410 | 10500794 | C-reactive protein abnormal | |
1050079410 | 10500794 | Chest pain | |
1050079410 | 10500794 | Drug dose omission | |
1050079410 | 10500794 | Dry mouth | |
1050079410 | 10500794 | Dyspnoea | |
1050079410 | 10500794 | Erysipelas | |
1050079410 | 10500794 | Erythema | |
1050079410 | 10500794 | Fall | |
1050079410 | 10500794 | Hypokalaemia | |
1050079410 | 10500794 | Joint injury | |
1050079410 | 10500794 | Malaise | |
1050079410 | 10500794 | Musculoskeletal pain | |
1050079410 | 10500794 | Nail injury | |
1050079410 | 10500794 | Nausea | |
1050079410 | 10500794 | Peripheral swelling | |
1050079410 | 10500794 | Pyrexia | |
1050079410 | 10500794 | Sepsis | |
1050079410 | 10500794 | Skin warm | |
1050079410 | 10500794 | Wound 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 |
---|---|---|---|---|---|---|
1050079410 | 10500794 | 1 | 20140520 | 0 | ||
1050079410 | 10500794 | 3 | 2003 | 0 | ||
1050079410 | 10500794 | 5 | 2012 | 0 |