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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126741262 | 12674126 | 2 | F | 20160817 | 20160818 | 20160822 | 20160901 | PER | US-PFIZER INC-2016394351 | PFIZER | 82.00 | YR | M | Y | 0.00000 | 20160901 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126741262 | 12674126 | 1 | PS | NEURONTIN | GABAPENTIN | 1 | Oral | 300 MG, 2X/DAY (100 MG CAPSULES THREE CAPSULES TWO TIMES A DAY) | U | 20235 | 300 | MG | CAPSULE, HARD | BID | |||||
| 126741262 | 12674126 | 2 | SS | NEURONTIN | GABAPENTIN | 1 | Oral | 3 CAPSULES FOR ONE DAY | U | 20235 | 3 | DF | CAPSULE, HARD | ||||||
| 126741262 | 12674126 | 3 | SS | NEURONTIN | GABAPENTIN | 1 | Oral | ONE CAPSULES FOR ONE DAY | U | 20235 | 1 | DF | CAPSULE, HARD | ||||||
| 126741262 | 12674126 | 4 | C | PRILOSEC | OMEPRAZOLE MAGNESIUM | 1 | TOOK ONE A DAY FOR 14 DAYS | 0 | 1 | DF | |||||||||
| 126741262 | 12674126 | 5 | C | PREDNISONE. | PREDNISONE | 1 | TOOK A TAPERING DOSE FOR 6 CONSECUTIVE DAYS. | 0 | |||||||||||
| 126741262 | 12674126 | 6 | C | METOPROLOL. | METOPROLOL | 1 | 50 MG, UNK | 0 | 50 | MG | |||||||||
| 126741262 | 12674126 | 7 | C | CRESTOR | ROSUVASTATIN CALCIUM | 1 | 5 MG, UNK | 0 | 5 | MG |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126741262 | 12674126 | 1 | Nerve compression |
| 126741262 | 12674126 | 5 | Nerve compression |
| 126741262 | 12674126 | 6 | Blood pressure abnormal |
| 126741262 | 12674126 | 7 | Blood cholesterol increased |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126741262 | 12674126 | Abdominal discomfort | |
| 126741262 | 12674126 | Abdominal distension | |
| 126741262 | 12674126 | Anxiety | |
| 126741262 | 12674126 | Circumstance or information capable of leading to medication error | |
| 126741262 | 12674126 | Disorientation | |
| 126741262 | 12674126 | Flushing | |
| 126741262 | 12674126 | Pain | |
| 126741262 | 12674126 | Product use issue | |
| 126741262 | 12674126 | Sleep disorder |
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 |
|---|---|---|---|---|---|---|
| 126741262 | 12674126 | 1 | 20160727 | 0 | ||
| 126741262 | 12674126 | 3 | 20160817 | 0 | ||
| 126741262 | 12674126 | 5 | 20160727 | 201608 | 0 |