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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126683181 | 12668318 | 1 | I | 2015 | 20160816 | 20160819 | 20160819 | EXP | PHHY2016VE113988 | NOVARTIS | 0.00 | F | Y | 0.00000 | 20160819 | CN | VE | VE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126683181 | 12668318 | 1 | PS | ACLASTA | ZOLEDRONIC ACID | 1 | Intravenous (not otherwise specified) | 5 MG, Q12MO | 21817 | 5 | MG | SOLUTION FOR INJECTION | |||||||
126683181 | 12668318 | 2 | C | CALCIBON /03134501/ | 2 | Unknown | 1 DF, QD | U | 0 | 1 | DF | CAPSULE | QD | ||||||
126683181 | 12668318 | 3 | C | VITAMIN B-1 | THIAMINE | 1 | Unknown | ON ALTERNATE DAYS, EVERY 1 AND A HALF MONTH OR 40 DAYS, IN 6 DOSES | U | 0 | |||||||||
126683181 | 12668318 | 4 | C | VITAMIN B12 | CYANOCOBALAMIN | 1 | Unknown | ON ALTERNATE DAYS, EVERY 1 AND A HALF MONTH OR 40 DAYS, IN 6 DOSES | U | 0 | |||||||||
126683181 | 12668318 | 5 | C | VITAMIN B6 | PYRIDOXINE HYDROCHLORIDE | 1 | Unknown | ON ALTERNATE DAYS, EVERY 1 AND A HALF MONTH OR 40 DAYS, IN 6 DOSES | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126683181 | 12668318 | 1 | Asthenia |
126683181 | 12668318 | 2 | Bone disorder |
126683181 | 12668318 | 3 | Vitamin B complex deficiency |
126683181 | 12668318 | 4 | Vitamin B complex deficiency |
126683181 | 12668318 | 5 | Vitamin B complex deficiency |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126683181 | 12668318 | LT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126683181 | 12668318 | Apparent death | |
126683181 | 12668318 | Asthenia | |
126683181 | 12668318 | Depressed mood | |
126683181 | 12668318 | Gastric disorder | |
126683181 | 12668318 | Gastrointestinal disorder | |
126683181 | 12668318 | Malaise | |
126683181 | 12668318 | Product use issue | |
126683181 | 12668318 | Weight decreased |
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 |
---|---|---|---|---|---|---|
126683181 | 12668318 | 1 | 2015 | 2015 | 0 |