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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127250931 | 12725093 | 1 | I | 20160620 | 20160825 | 20160908 | 20160908 | EXP | GB-MHRA-EYC 00144093 | GB-TEVA-688589ACC | TEVA | 46.00 | YR | M | Y | 76.00000 | KG | 20160908 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127250931 | 12725093 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | 2 DOSAGE FORMS DAILY; | 20 | DF | N | U | 74124 | 2 | DF | TABLET | QD |
Indications of drugs used
no results found |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127250931 | 12725093 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127250931 | 12725093 | Dry eye | |
127250931 | 12725093 | Fatigue | |
127250931 | 12725093 | Mouth ulceration | |
127250931 | 12725093 | Tendon pain | |
127250931 | 12725093 | Tendonitis |
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 |
---|---|---|---|---|---|---|
127250931 | 12725093 | 1 | 20160610 | 20160620 | 0 |