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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125502702 | 12550270 | 2 | F | 20160607 | 20160727 | 20160712 | 20160803 | EXP | PHHY2016LT081940 | NOVARTIS | 76.00 | YR | F | Y | 43.00000 | KG | 20160803 | OT | LT | LT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125502702 | 12550270 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 5 MG/100ML, Q12MO | 5 | MG | 21817 | 5 | MG | SOLUTION FOR INJECTION | |||||
| 125502702 | 12550270 | 2 | C | MOXONIDINE | MOXONIDINE | 1 | Unknown | 0.3 MG, UNK | U | 0 | .3 | MG | |||||||
| 125502702 | 12550270 | 3 | C | LOKREN | BETAXOLOL HYDROCHLORIDE | 1 | Unknown | 10 MG, UNK | U | 0 | 10 | MG | |||||||
| 125502702 | 12550270 | 4 | C | BETALOC | METOPROLOL TARTRATE | 1 | Unknown | 25 MG, UNK | U | 0 | 25 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125502702 | 12550270 | 1 | Osteoporosis |
| 125502702 | 12550270 | 2 | Hypertension |
| 125502702 | 12550270 | 3 | Hypertension |
| 125502702 | 12550270 | 4 | Hypertension |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125502702 | 12550270 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125502702 | 12550270 | Anaemia | |
| 125502702 | 12550270 | Blood iron decreased | |
| 125502702 | 12550270 | C-reactive protein increased | |
| 125502702 | 12550270 | Headache | |
| 125502702 | 12550270 | Pain | |
| 125502702 | 12550270 | Pleural effusion | |
| 125502702 | 12550270 | Pyrexia | |
| 125502702 | 12550270 | Red blood cell sedimentation rate increased |
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 |
|---|---|---|---|---|---|---|
| 125502702 | 12550270 | 1 | 20160607 | 20160607 | 0 |