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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122636435 | 12263643 | 5 | F | 20160907 | 20160413 | 20160913 | PER | PHEH2016US008953 | NOVARTIS | 0.00 | M | Y | 106.58000 | KG | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122636435 | 12263643 | 1 | PS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | 0.0625 MG(0.25ML), QOD (WEEKS 1-2) | 125290 | .062 | MG | SOLUTION FOR INJECTION | |||||||
| 122636435 | 12263643 | 2 | SS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | 0.125 MG(0.5ML), QOD (WEEKS 3-4) | 125290 | .125 | MG | SOLUTION FOR INJECTION | |||||||
| 122636435 | 12263643 | 3 | SS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | 0.1875MG (0.75ML),QOD (WEEKS 5-6) | 125290 | .187 | MG | SOLUTION FOR INJECTION | |||||||
| 122636435 | 12263643 | 4 | SS | EXTAVIA | INTERFERON BETA-1B | 1 | Subcutaneous | 0.25MG (1 ML),QOD (WEEKS 7+) | 125290 | .25 | MG | SOLUTION FOR INJECTION |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122636435 | 12263643 | 1 | Multiple sclerosis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122636435 | 12263643 | Feeling hot | |
| 122636435 | 12263643 | Injection site extravasation | |
| 122636435 | 12263643 | Injection site nerve damage | |
| 122636435 | 12263643 | Injection site pain | |
| 122636435 | 12263643 | Paraesthesia | |
| 122636435 | 12263643 | 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 |
|---|---|---|---|---|---|---|
| 122636435 | 12263643 | 1 | 20160406 | 0 |