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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126059112 | 12605911 | 2 | F | 20160615 | 20160810 | 20160729 | 20160817 | EXP | US-AMGEN-USASL2016095249 | AMGEN | 61.00 | YR | A | F | Y | 61.00000 | KG | 20160817 | CN | US | US |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126059112 | 12605911 | 1 | PS | PROLIA | DENOSUMAB | 1 | Unknown | UNK | 125320 | SOLUTION FOR INJECTION | |||||||||
126059112 | 12605911 | 2 | C | PROZAC | FLUOXETINE HYDROCHLORIDE | 1 | UNK | 0 | |||||||||||
126059112 | 12605911 | 3 | C | ZORVOLEX | DICLOFENAC | 1 | UNK | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126059112 | 12605911 | 1 | Osteoporosis postmenopausal |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126059112 | 12605911 | OT |
126059112 | 12605911 | DE |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126059112 | 12605911 | Anal incontinence | |
126059112 | 12605911 | Asthenia | |
126059112 | 12605911 | Bone pain | |
126059112 | 12605911 | Death | |
126059112 | 12605911 | Infection | |
126059112 | 12605911 | Malaise | |
126059112 | 12605911 | Mobility decreased | |
126059112 | 12605911 | Nausea | |
126059112 | 12605911 | Pain |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |