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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126722021 | 12672202 | 1 | I | 20160720 | 20160816 | 20160822 | 20160822 | EXP | US-PFIZER INC-2016391289 | PFIZER | 63.00 | YR | F | Y | 52.16000 | KG | 20160822 | CN | US | US |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126722021 | 12672202 | 1 | PS | FLAGYL | METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE | 1 | Oral | 250 MG, 3X/DAY | 1500 | MG | Y | 12623 | 250 | MG | FILM-COATED TABLET | TID | |||
| 126722021 | 12672202 | 2 | SS | FLAGYL | METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE | 1 | 1500 | MG | Y | 12623 | FILM-COATED TABLET | ||||||||
| 126722021 | 12672202 | 3 | SS | FLAGYL | METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | UNK | Y | 18353 | SOLUTION FOR INJECTION | ||||||||
| 126722021 | 12672202 | 4 | SS | FLAGYL | METRONIDAZOLEMETRONIDAZOLE HYDROCHLORIDE | 1 | Y | 18353 | SOLUTION FOR INJECTION | ||||||||||
| 126722021 | 12672202 | 5 | C | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | 875 MG, 2X/DAY | 0 | 875 | MG | BID | ||||||||
| 126722021 | 12672202 | 6 | C | KEFLEX | CEPHALEXIN | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126722021 | 12672202 | 1 | Diverticulitis |
| 126722021 | 12672202 | 2 | Abdominal abscess |
| 126722021 | 12672202 | 3 | Diverticulitis |
| 126722021 | 12672202 | 4 | Abdominal abscess |
| 126722021 | 12672202 | 5 | Antibiotic prophylaxis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126722021 | 12672202 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126722021 | 12672202 | Drug intolerance | |
| 126722021 | 12672202 | Dysgeusia | |
| 126722021 | 12672202 | Headache | |
| 126722021 | 12672202 | Neuromyopathy | |
| 126722021 | 12672202 | Pain |
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 |
|---|---|---|---|---|---|---|
| 126722021 | 12672202 | 1 | 20160719 | 20160814 | 0 |