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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125226211 | 12522621 | 1 | I | 20160624 | 20160701 | 20160701 | EXP | PHHY2016BR089770 | NOVARTIS | 0.00 | F | Y | 78.00000 | KG | 20160701 | MD | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125226211 | 12522621 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 5 MG, UNK | 21817 | 5 | MG | SOLUTION FOR INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125226211 | 12522621 | 1 | Osteoporosis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125226211 | 12522621 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125226211 | 12522621 | Arthralgia | |
| 125226211 | 12522621 | Grip strength decreased | |
| 125226211 | 12522621 | Hypersensitivity | |
| 125226211 | 12522621 | Hypoaesthesia | |
| 125226211 | 12522621 | Neck pain | |
| 125226211 | 12522621 | Pain | |
| 125226211 | 12522621 | Pain in extremity | |
| 125226211 | 12522621 | Speech disorder | |
| 125226211 | 12522621 | Vertebral artery stenosis | |
| 125226211 | 12522621 | Vomiting | |
| 125226211 | 12522621 | Weight decreased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |