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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282283 | 6276604 | I | 5282283-1 | 20070208 | 20070319 | 20070331 | EXP | GB-PFIZER INC-2007023354 | PFIZER INC | 49 | YR | F | Y | 87 | KG | 20070330 | OT | UNITED KINGDOM |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 5282283 | 1008316816 | PS | GABAPENTIN | 1 | ORAL | 020235 | |||||
| 5282283 | 1008316817 | C | ACETYLSALICYLIC ACID SRT | 1 | |||||||
| 5282283 | 1008316818 | C | CELECOXIB | 2 | |||||||
| 5282283 | 1008316819 | C | DIHYDROCODEINE BITARTRATE INJ | 1 | ORAL | ||||||
| 5282283 | 1008316820 | C | ACETAMINOPHEN | 1 | ORAL | ||||||
| 5282283 | 1008316821 | C | RABEPRAZOLE SODIUM | 1 |
Indications of drugs used
| Event ID | DRUG SEQ | INDI PT |
|---|---|---|
| 5282283 | 1008316816 | NEURALGIA |
Outcome of event
| Event ID | OUTC COD |
|---|---|
| 5282283 | OT |
Reactions reported
| Event ID | PT |
|---|---|
| 5282283 | MIGRAINE |
| 5282283 | OCULAR HYPERAEMIA |
| 5282283 | PARAESTHESIA |
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 |
|---|---|---|---|---|---|
| 5282283 | 1008316816 | 20070207 | 20070217 |