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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122766835 | 12276683 | 5 | F | 20160805 | 20160418 | 20160812 | PER | US-PFIZER INC-2016197421 | PFIZER | 72.00 | YR | F | Y | 0.00000 | 20160812 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122766835 | 12276683 | 1 | PS | NEURONTIN | GABAPENTIN | 1 | 600 MG, 4X/DAY | Y | 20235 | 600 | MG | QID | |||||||
| 122766835 | 12276683 | 2 | SS | NEURONTIN | GABAPENTIN | 1 | 600 MG, 4X/DAY | Y | 20235 | 600 | MG | QID | |||||||
| 122766835 | 12276683 | 3 | SS | NEURONTIN | GABAPENTIN | 1 | Y | 20235 | |||||||||||
| 122766835 | 12276683 | 4 | C | RANIT | 2 | 300 MG, DAILY (150 MG, 1-TAB X 2 DAILY ) | 0 | 150 | MG | TABLET | BID | ||||||||
| 122766835 | 12276683 | 5 | C | MAGNESIUM | MAGNESIUM | 1 | 250 MG, DAILY | 0 | 250 | MG | |||||||||
| 122766835 | 12276683 | 6 | C | SPIRONOLACTONE. | SPIRONOLACTONE | 1 | 25 MG, DAILY | 0 | 25 | MG | |||||||||
| 122766835 | 12276683 | 7 | C | SOTALOL. | SOTALOL | 1 | 80 MG, 2X/DAY | 0 | 80 | MG | BID | ||||||||
| 122766835 | 12276683 | 8 | C | OXYCODONE | OXYCODONE | 1 | AS NEEDED (10/325 MG EVERY 6 HRS AS NEEDED) | 0 | |||||||||||
| 122766835 | 12276683 | 9 | C | CITALOPRAM | CITALOPRAM HYDROBROMIDE | 1 | 40 MG, DAILY | 0 | 40 | MG | TABLET | ||||||||
| 122766835 | 12276683 | 10 | C | TRAZODONE | TRAZODONE HYDROCHLORIDE | 1 | 150 MG, 1X/DAY (150 MG 1 TAB BEDTIME) | 0 | 150 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122766835 | 12276683 | 1 | Pain |
| 122766835 | 12276683 | 2 | Hypoaesthesia |
| 122766835 | 12276683 | 3 | Paraesthesia |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122766835 | 12276683 | Drug ineffective for unapproved indication |
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 |
|---|---|---|---|---|---|---|
| 122766835 | 12276683 | 1 | 201511 | 0 | ||
| 122766835 | 12276683 | 2 | 20160120 | 201601 | 0 | |
| 122766835 | 12276683 | 4 | 201605 | 0 | ||
| 122766835 | 12276683 | 5 | 201504 | 0 | ||
| 122766835 | 12276683 | 7 | 201504 | 0 | ||
| 122766835 | 12276683 | 9 | 201504 | 0 | ||
| 122766835 | 12276683 | 10 | 201504 | 0 |