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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126031071 | 12603107 | 1 | I | 20160704 | 20160722 | 20160728 | 20160728 | EXP | GB-MHRA-ADR 23568810 | PHHY2016GB101716 | SANDOZ | 65.00 | YR | F | Y | 80.00000 | KG | 20160728 | OT | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126031071 | 12603107 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Intravenous (not otherwise specified) | 300 MG, UNK | Y | U | 5113KH | 64076 | 300 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126031071 | 12603107 | 1 | Lower respiratory tract infection |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126031071 | 12603107 | LT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126031071 | 12603107 | Anaphylactic reaction | |
126031071 | 12603107 | Pulseless electrical activity |
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 |
---|---|---|---|---|---|---|
126031071 | 12603107 | 1 | 20160704 | 20160704 | 0 |