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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127593481 | 12759348 | 1 | I | 20160915 | 0 | 20160919 | 20160919 | DIR | US-FDA-350959 | FDA-CTU | 60.00 | YR | F | N | 76.50000 | KG | 20160919 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127593481 | 12759348 | 1 | PS | NEURONTIN | GABAPENTIN | 1 | Oral | Y | D | 20170914 | 0 | 30 | G | HS | |||||
| 127593481 | 12759348 | 2 | C | PROTONIX | PANTOPRAZOLE SODIUM | 1 | 0 | ||||||||||||
| 127593481 | 12759348 | 3 | C | ESTRADIOL. | ESTRADIOL | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127593481 | 12759348 | 1 | Intervertebral disc protrusion |
| 127593481 | 12759348 | 1 | Neuralgia |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127593481 | 12759348 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127593481 | 12759348 | Abnormal behaviour | |
| 127593481 | 12759348 | Anger | |
| 127593481 | 12759348 | Asthenia | |
| 127593481 | 12759348 | Fatigue | |
| 127593481 | 12759348 | Irritability |
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 |
|---|---|---|---|---|---|---|
| 127593481 | 12759348 | 1 | 20160914 | 20160917 | 0 |