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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125810031 | 12581003 | 1 | I | 20160707 | 20160708 | 20160721 | 20160721 | PER | US-BAYER-2016-136357 | BAYER | 46.22 | YR | F | Y | 0.00000 | 20160721 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125810031 | 12581003 | 1 | PS | BETASERON | INTERFERON BETA-1B | 1 | Subcutaneous | 0.25 ML, UNK | 52197A | 103471 | .25 | ML | POWDER AND SOLVENT FOR SOLUTION FOR INJECTION |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125810031 | 12581003 | 1 | Multiple sclerosis |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125810031 | 12581003 | Drug dose omission | |
125810031 | 12581003 | Incorrect product storage |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |