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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117601372 | 11760137 | 2 | F | 20150921 | 20160712 | 20151120 | 20160726 | EXP | IT-AUROBINDO-AUR-APL-2015-10316 | AUROBINDO | 49.88 | YR | M | Y | 0.00000 | 20160726 | OT | IT | IT |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
117601372 | 11760137 | 1 | PS | AMOXICILLIN. | AMOXICILLIN | 1 | Oral | 2 DF DAILY | Y | U | 65256 | 2 | DF |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
117601372 | 11760137 | 1 | Tooth disorder |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
117601372 | 11760137 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
117601372 | 11760137 | Erythema | |
117601372 | 11760137 | Eye irritation | |
117601372 | 11760137 | Laryngeal oedema | |
117601372 | 11760137 | Lip oedema | |
117601372 | 11760137 | Pharyngeal oedema | |
117601372 | 11760137 | Pruritus generalised | |
117601372 | 11760137 | Urticaria |
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 |
---|---|---|---|---|---|---|
117601372 | 11760137 | 1 | 20150915 | 20150921 | 0 |