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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116293105 | 11629310 | 5 | F | 2015 | 20160913 | 20151014 | 20160919 | EXP | US-PFIZER INC-2015339994 | PFIZER | 65.00 | YR | F | Y | 58.50000 | KG | 20160919 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116293105 | 11629310 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 75 MG, 1X/DAY | D | 21446 | 75 | MG | CAPSULE, HARD | QD | |||||
| 116293105 | 11629310 | 2 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 2X/DAY MORNING AND NIGHT | D | N51077 | 21446 | 150 | MG | CAPSULE, HARD | BID | ||||
| 116293105 | 11629310 | 3 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 25 MG, 1X/DAY | 0 | 25 | MG | TABLET | QD | |||||||
| 116293105 | 11629310 | 4 | C | CARVEDILOL. | CARVEDILOL | 1 | 25 MG, 2X/DAY | 0 | 25 | MG | TABLET | BID | |||||||
| 116293105 | 11629310 | 5 | C | HYDROCODONE/ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE | 1 | [HYDROCODONE 10/ PARACETAMOL 500], UNK | 0 | 1 | DF | TABLET | ||||||||
| 116293105 | 11629310 | 6 | C | HYDROCODONE/ACETAMINOPHEN | ACETAMINOPHENHYDROCODONE | 1 | [HYDROCODONE 10 /PARACETAMOL 325], 4X/DAY AS NEEDED | 0 | 1 | DF | TABLET | QID | |||||||
| 116293105 | 11629310 | 7 | C | CLONAZEPAM. | CLONAZEPAM | 1 | 1 MG, 2X/DAY (IF NEEDED) | 0 | 1 | MG | TABLET | BID | |||||||
| 116293105 | 11629310 | 8 | C | AMBIEN | ZOLPIDEM TARTRATE | 1 | UNK | 0 | |||||||||||
| 116293105 | 11629310 | 9 | C | ZOLPIDEM TARTRATE. | ZOLPIDEM TARTRATE | 1 | 10 MG, 1X/DAY (AT BEDTIME) | 0 | 10 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116293105 | 11629310 | 1 | Nerve injury |
| 116293105 | 11629310 | 2 | Herpes zoster |
| 116293105 | 11629310 | 3 | Fluid retention |
| 116293105 | 11629310 | 4 | Blood pressure abnormal |
| 116293105 | 11629310 | 5 | Pain |
| 116293105 | 11629310 | 7 | Anxiety |
| 116293105 | 11629310 | 9 | Sleep disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 116293105 | 11629310 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116293105 | 11629310 | Activities of daily living impaired | |
| 116293105 | 11629310 | Asthenia | |
| 116293105 | 11629310 | Bedridden | |
| 116293105 | 11629310 | Cataract | |
| 116293105 | 11629310 | Drug dose omission | |
| 116293105 | 11629310 | Drug ineffective | |
| 116293105 | 11629310 | Gait disturbance | |
| 116293105 | 11629310 | Impaired work ability | |
| 116293105 | 11629310 | Insomnia | |
| 116293105 | 11629310 | Malaise | |
| 116293105 | 11629310 | Pain | |
| 116293105 | 11629310 | Peripheral swelling | |
| 116293105 | 11629310 | Pruritus | |
| 116293105 | 11629310 | Somnolence |
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 |
|---|---|---|---|---|---|---|
| 116293105 | 11629310 | 2 | 2008 | 0 |