Person who experienced the adverse event (patient)
Event ID | CASE | I F COD | FOLL SEQ | IMAGE | EVENT DT | MFR DT | FDA DT | REPT COD | MFR NUM | MFR SNDR | AGE | AGE COD | GNDR COD | E SUB | WT | WT COD | REPT DT | OCCP COD | DEATH DT | TO MFR | CONFID | REPORTER COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5329797 | 6317668 | I | 5329797-3 | 20070516 | 20070517 | DIR | 62 | YR | M | N | 162 | LBS | 20070516 | CN | N | Y | UNITED STATES |
Drug(s) used by person
Event ID | DRUG SEQ | ROLE COD | DRUGNAME | VAL VBM | ROUTE | DOSE VBM | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM |
---|---|---|---|---|---|---|---|---|---|---|---|
5329797 | 1008497769 | PS | LEVAQUIN | 1 | ORAL | 500MG 2 / DAY PO | Y | ||||
5329797 | 1008504116 | SS | CIPROFLOXACIN | 1 | ORAL | 500MG 2/DAY PO | D | Y |
Indications of drugs used
Event ID | DRUG SEQ | INDI PT |
---|---|---|
5329797 | 1008497769 | GASTROINTESTINAL INFECTION |
5329797 | 1008504116 | GASTROINTESTINAL INFECTION |
Outcome of event
Event ID | OUTC COD |
---|---|
5329797 | OT |
Reactions reported
Event ID | PT |
---|---|
5329797 | FATIGUE |
5329797 | IMPAIRED WORK ABILITY |
5329797 | LETHARGY |
5329797 | LIGAMENT DISORDER |
5329797 | LIGAMENT RUPTURE |
5329797 | MENTAL IMPAIRMENT |
5329797 | PARAESTHESIA |
5329797 | SOMNOLENCE |
5329797 | TENDON PAIN |
5329797 | TINNITUS |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
---|---|---|---|---|---|
5329797 | 1008497769 | 20070309 | 20070313 | 5 | DAY |
5329797 | 1008504116 | 20070510 | 20070516 |