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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
106887782 | 10688778 | 2 | F | 20160704 | 20150103 | 20160716 | EXP | SE-AUROBINDO-AUR-APL-2014-13472 | AUROBINDO | 83.00 | YR | F | Y | 0.00000 | 20160716 | OT | SE | SE |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
106887782 | 10688778 | 1 | PS | Metoprolol Film-coated Tablet | METOPROLOL | 1 | Oral | 25 MG, UNK | U | U | 77739 | 25 | MG | FILM-COATED TABLET | |||||
106887782 | 10688778 | 2 | SS | BISOPROLOL | BISOPROLOL | 1 | Oral | 5 MG, UNK | U | U | 0 | 5 | MG | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
106887782 | 10688778 | 1 | Product used for unknown indication |
106887782 | 10688778 | 2 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
106887782 | 10688778 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
106887782 | 10688778 | Bradycardia | |
106887782 | 10688778 | Drug prescribing error | |
106887782 | 10688778 | Dyspnoea | |
106887782 | 10688778 | Fatigue |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |