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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127027621 | 12702762 | 1 | I | 20160615 | 20160818 | 20160831 | 20160831 | EXP | GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-122819 | RANBAXY | 48.00 | YR | M | Y | 80.00000 | KG | 20160831 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127027621 | 12702762 | 1 | PS | CIPROFLOXACIN. | CIPROFLOXACIN | 1 | Oral | 500 MG, BID | 5000 | MG | N | U | 75747 | 500 | MG | Q12H | |||
127027621 | 12702762 | 2 | C | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Unknown | UNK | U | U | 0 | ||||||||
127027621 | 12702762 | 3 | C | DOXYCYCLINE. | DOXYCYCLINE | 1 | Unknown | UNK | U | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127027621 | 12702762 | 1 | Diverticulitis |
127027621 | 12702762 | 2 | Product used for unknown indication |
127027621 | 12702762 | 3 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127027621 | 12702762 | OT |
127027621 | 12702762 | DS |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127027621 | 12702762 | Anxiety | |
127027621 | 12702762 | Arthritis | |
127027621 | 12702762 | Burning sensation | |
127027621 | 12702762 | Diarrhoea | |
127027621 | 12702762 | Dyspnoea | |
127027621 | 12702762 | Gastrointestinal disorder | |
127027621 | 12702762 | Insomnia | |
127027621 | 12702762 | Intervertebral disc disorder | |
127027621 | 12702762 | Nausea | |
127027621 | 12702762 | 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 |
---|---|---|---|---|---|---|
127027621 | 12702762 | 1 | 20160610 | 20160615 | 0 |