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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100080752 | 10008075 | 2 | F | 2013 | 20140327 | 20140313 | 20140331 | EXP | PHHY2014NL030419 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20140331 | N | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 100080752 | 10008075 | 1 | PS | ACLASTA | 1 | INTRAVENOUS | 5 MG, UNK (1 PER 52 WEEKS) | U | S0216 | 21817 | 5 | MG | SOLUTION FOR INJECTION | ||||||
| 100080752 | 10008075 | 2 | SS | ACLASTA | 1 | INTRAVENOUS | 5 MG, UNK | U | S0278 | 21817 | 5 | MG | SOLUTION FOR INJECTION | ||||||
| 100080752 | 10008075 | 3 | SS | ACLASTA | 1 | INTRAVENOUS | 5 MG, UNK | U | 16FF0062 | 21817 | 5 | MG | SOLUTION FOR INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 100080752 | 10008075 | 1 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 100080752 | 10008075 | OT |
| 100080752 | 10008075 | DE |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 100080752 | 10008075 | Acetabulum fracture | |
| 100080752 | 10008075 | Blood creatinine increased | |
| 100080752 | 10008075 | C-reactive protein increased | |
| 100080752 | 10008075 | Cerebral haemorrhage | |
| 100080752 | 10008075 | Decubitus ulcer | |
| 100080752 | 10008075 | Fall | |
| 100080752 | 10008075 | Haemoglobin decreased | |
| 100080752 | 10008075 | Platelet count decreased | |
| 100080752 | 10008075 | Prothrombin time prolonged |
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 |
|---|---|---|---|---|---|---|
| 100080752 | 10008075 | 1 | 201102 | 0 | ||
| 100080752 | 10008075 | 2 | 20120316 | 0 | ||
| 100080752 | 10008075 | 3 | 20130318 | 0 |