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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127020641 | 12702064 | 1 | I | 20160620 | 20160825 | 20160831 | 20160831 | EXP | GB-MHRA-EYC 00144093 | GB-DRREDDYS-GER/UKI/16/0082808 | DR REDDYS | 46.00 | YR | M | Y | 76.00000 | KG | 20160831 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127020641 | 12702064 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | 20 | DF | N | U | UNKNOWN | 75593 | 2 | DF | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127020641 | 12702064 | 1 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127020641 | 12702064 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127020641 | 12702064 | Dry eye | |
127020641 | 12702064 | Fatigue | |
127020641 | 12702064 | Mouth ulceration | |
127020641 | 12702064 | Tendon pain | |
127020641 | 12702064 | 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 |
---|---|---|---|---|---|---|
127020641 | 12702064 | 1 | 20160610 | 20160620 | 0 |