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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 4338027 | 5722835 | I | 4338027-0 | 20040208 | 20040326 | 20040407 | EXP | 2004206088FR | PFIZER INC. | 8 | YR | F | N | 34 | KG | 20040402 | OT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 4338027 | 1004783693 | PS | VANTIN | 1 | Y | D | 50674 | ||||
| 4338027 | 1004795907 | SS | OFLOXACIN | 1 | ORAL | 400 MG, DAILY, ORAL | U | U | |||
| 4338027 | 1004795909 | C | AUGMENTAN ORAL | 2 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 4338027 | 1004783693 | EAR INFECTION |
| 4338027 | 1004795907 | EAR INFECTION |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 4338027 | HO |
Reactions reported
| Event ID | PT |
|---|---|
| 4338027 | ANOREXIA |
| 4338027 | BALANCE DISORDER |
| 4338027 | C-REACTIVE PROTEIN INCREASED |
| 4338027 | DIARRHOEA |
| 4338027 | FOOD AVERSION |
| 4338027 | GASTROINTESTINAL DISORDER |
| 4338027 | INTRACRANIAL PRESSURE INCREASED |
| 4338027 | MONOCYTE PERCENTAGE INCREASED |
| 4338027 | MULTIPLE SCLEROSIS |
| 4338027 | NAUSEA |
| 4338027 | PARAESTHESIA |
| 4338027 | RETINAL OEDEMA |
| 4338027 | VITH NERVE PARALYSIS |
Reporting Sources (this data is often not reported and may therefore be missing here)
| Event ID | RPSR COD |
|---|---|
| 4338027 | FGN |
| 4338027 | HP |
| 4338027 | OTH |
Therapies reported
| Event ID | DRUG SEQ | START DT | END DT | DUR | DUR COD |
|---|---|---|---|---|---|
| 4338027 | 1004783693 | 20040208 | 20040216 | ||
| 4338027 | 1004795907 | 20040205 | 20040212 |