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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126074222 | 12607422 | 2 | F | 2012 | 20160727 | 20160729 | 20160802 | EXP | US-PFIZER INC-2016365286 | PFIZER | 75.00 | YR | F | Y | 78.20000 | KG | 20160802 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126074222 | 12607422 | 1 | PS | NEURONTIN | GABAPENTIN | 1 | UNK | Y | 20235 | ||||||||||
| 126074222 | 12607422 | 2 | SS | NEURONTIN | GABAPENTIN | 1 | 600MG IN MORNING, MIDDAY AND AT NIGHT | Y | 20235 | 600 | MG | TID | |||||||
| 126074222 | 12607422 | 3 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0.01 MG, DAILY | 0 | .01 | MG | |||||||||
| 126074222 | 12607422 | 4 | C | RAMIPRIL. | RAMIPRIL | 1 | 0 | ||||||||||||
| 126074222 | 12607422 | 5 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | 500 MG, 1X/DAY | 0 | 500 | MG | QD | ||||||||
| 126074222 | 12607422 | 6 | C | LIPITOR | ATORVASTATIN CALCIUM | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126074222 | 12607422 | 1 | Back pain |
| 126074222 | 12607422 | 3 | Thyroid cancer |
| 126074222 | 12607422 | 5 | Diabetes mellitus |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126074222 | 12607422 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126074222 | 12607422 | Blood glucose decreased | |
| 126074222 | 12607422 | Diarrhoea | |
| 126074222 | 12607422 | Dyspnoea | |
| 126074222 | 12607422 | Heart rate increased | |
| 126074222 | 12607422 | Intentional product use issue | |
| 126074222 | 12607422 | Nausea | |
| 126074222 | 12607422 | Product use issue | |
| 126074222 | 12607422 | Pruritus |
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 |
|---|---|---|---|---|---|---|
| 126074222 | 12607422 | 1 | 2012 | 0 | ||
| 126074222 | 12607422 | 2 | 20160710 | 0 |