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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126061703 | 12606170 | 3 | F | 20160919 | 20160729 | 20160922 | PER | US-PFIZER INC-2016365376 | PFIZER | 0.00 | M | Y | 0.00000 | 20160922 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126061703 | 12606170 | 1 | PS | LYRICA | PREGABALIN | 1 | 150 MG, 2X/DAY | U | 21446 | 150 | MG | BID | |||||||
| 126061703 | 12606170 | 2 | SS | LYRICA | PREGABALIN | 1 | 150 MG, 1X/DAY | U | 21446 | 150 | MG | QD | |||||||
| 126061703 | 12606170 | 3 | SS | GABAPENTIN. | GABAPENTIN | 1 | UNK, 1X/DAY (IN THE EVENING) | U | 20235 | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126061703 | 12606170 | 1 | Diabetic neuropathy |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126061703 | 12606170 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126061703 | 12606170 | Anxiety | |
| 126061703 | 12606170 | Insomnia | |
| 126061703 | 12606170 | Suicidal ideation |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |