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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127654742 | 12765474 | 2 | F | 20160830 | 20160920 | 20160921 | 20160923 | EXP | IT-AUROBINDO-AUR-APL-2016-11908 | AUROBINDO | 47.75 | YR | F | Y | 0.00000 | 20160923 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127654742 | 12765474 | 1 | PS | IBUPROFEN. | IBUPROFEN | 1 | Oral | 1 DF, AS NECESSARY | Y | U | 70734 | 1 | DF | ||||||
127654742 | 12765474 | 2 | SS | AMOXICILLIN. | AMOXICILLIN | 1 | Unknown | 2 G, DAILY | Y | U | 0 | 2 | G |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127654742 | 12765474 | 1 | Pain |
127654742 | 12765474 | 2 | Tooth abscess |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127654742 | 12765474 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127654742 | 12765474 | 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 |
---|---|---|---|---|---|---|
127654742 | 12765474 | 1 | 20160824 | 20160829 | 0 | |
127654742 | 12765474 | 2 | 20160824 | 20160829 | 0 |