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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123537753 | 12353775 | 3 | F | 20160912 | 20160511 | 20160917 | EXP | PHEH2016US011209 | NOVARTIS | 0.00 | M | Y | 0.00000 | 20160918 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
123537753 | 12353775 | 1 | PS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | WEEK 1-2, 0.062 MG, (0.25 ML), QOD | 125290 | .062 | MG | SOLUTION FOR INJECTION | |||||||
123537753 | 12353775 | 2 | SS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | WEEK 3-4, 0.125 MG, (0.5 ML), QOD | 125290 | .125 | MG | SOLUTION FOR INJECTION | |||||||
123537753 | 12353775 | 3 | SS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | WEEK 5-6, 0.187 MG, (0.75 ML), QOD | 125290 | .187 | MG | SOLUTION FOR INJECTION | |||||||
123537753 | 12353775 | 4 | SS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | WEEK 7+, 0.25 MG, QOD | 125290 | .25 | MG | SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
123537753 | 12353775 | 1 | Multiple sclerosis |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
123537753 | 12353775 | HO |
123537753 | 12353775 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
123537753 | 12353775 | Blood glucose increased | |
123537753 | 12353775 | Cervical vertebral fracture | |
123537753 | 12353775 | Chills | |
123537753 | 12353775 | Depression | |
123537753 | 12353775 | Fall | |
123537753 | 12353775 | Injection site scar | |
123537753 | 12353775 | Memory impairment | |
123537753 | 12353775 | Nausea | |
123537753 | 12353775 | Product preparation error | |
123537753 | 12353775 | Restlessness | |
123537753 | 12353775 | Tremor |
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 |
---|---|---|---|---|---|---|
123537753 | 12353775 | 1 | 20160426 | 0 |