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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122023526 | 12202352 | 6 | F | 20160704 | 20160322 | 20160711 | EXP | PHHY2016BR037190 | NOVARTIS | 0.00 | F | Y | 76.00000 | KG | 20160711 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
122023526 | 12202352 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 1 DF, Q12MO | 21817 | 1 | DF | SOLUTION FOR INJECTION | |||||||
122023526 | 12202352 | 2 | SS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 1 DF, Q12MO | SC542 | 21817 | 1 | DF | SOLUTION FOR INJECTION | ||||||
122023526 | 12202352 | 3 | C | CALCIUM | CALCIUM | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
122023526 | 12202352 | 1 | Osteoporosis |
122023526 | 12202352 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
122023526 | 12202352 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
122023526 | 12202352 | Arthralgia | |
122023526 | 12202352 | Fall | |
122023526 | 12202352 | Inappropriate schedule of drug administration | |
122023526 | 12202352 | Influenza | |
122023526 | 12202352 | Intervertebral disc protrusion | |
122023526 | 12202352 | Lower limb fracture | |
122023526 | 12202352 | Malaise | |
122023526 | 12202352 | Pain | |
122023526 | 12202352 | Patient-device incompatibility | |
122023526 | 12202352 | Spinal pain | |
122023526 | 12202352 | Urinary tract infection | |
122023526 | 12202352 | Visual impairment |
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 |
---|---|---|---|---|---|---|
122023526 | 12202352 | 1 | 20150520 | 0 | ||
122023526 | 12202352 | 2 | 20160329 | 0 |