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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88383125 | 8838312 | 5 | F | 201209 | 20160920 | 20121012 | 20160923 | PER | US-PFIZER INC-2012252353 | PFIZER | 58.00 | YR | F | Y | 63.49000 | KG | 20160923 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 88383125 | 8838312 | 1 | PS | LYRICA | PREGABALIN | 1 | Oral | 75 MG, 3X/DAY | 21446 | 75 | MG | CAPSULE, HARD | TID | ||||||
| 88383125 | 8838312 | 2 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 2X/DAY | V121043 | 21446 | 150 | MG | CAPSULE, HARD | BID | |||||
| 88383125 | 8838312 | 3 | SS | LYRICA | PREGABALIN | 1 | Oral | 50 MG, UNK | 21446 | 50 | MG | CAPSULE, HARD | |||||||
| 88383125 | 8838312 | 4 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, UNK | 21446 | 150 | MG | CAPSULE, HARD | |||||||
| 88383125 | 8838312 | 5 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 3X/DAY | 21446 | 150 | MG | CAPSULE, HARD | TID | ||||||
| 88383125 | 8838312 | 6 | SS | LYRICA | PREGABALIN | 1 | Oral | 150 MG, 3X/DAY (CAPSULE 75 MG, 2 CAPSULES THREE TIMES A DAY ) | 21446 | 150 | MG | CAPSULE, HARD | TID | ||||||
| 88383125 | 8838312 | 7 | SS | LYRICA | PREGABALIN | 1 | 150 MG, UNK, (1-3 TIMES A DAY) | 21446 | 150 | MG | CAPSULE, HARD | ||||||||
| 88383125 | 8838312 | 8 | C | LISINOPRIL. | LISINOPRIL | 1 | 2.5 MG, 2X/DAY | 0 | 2.5 | MG | BID | ||||||||
| 88383125 | 8838312 | 9 | C | CARVEDILOL. | CARVEDILOL | 1 | 6.25 MG, 2X/DAY | 0 | 6.25 | MG | BID | ||||||||
| 88383125 | 8838312 | 10 | C | PLAVIX | CLOPIDOGREL BISULFATE | 1 | UNK | 0 | |||||||||||
| 88383125 | 8838312 | 11 | C | COREG | CARVEDILOL | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 88383125 | 8838312 | 1 | Pain in extremity |
| 88383125 | 8838312 | 2 | Intervertebral disc degeneration |
| 88383125 | 8838312 | 8 | Hypertension |
| 88383125 | 8838312 | 9 | Hypertension |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 88383125 | 8838312 | Drug ineffective | |
| 88383125 | 8838312 | Pain | |
| 88383125 | 8838312 | Poor quality drug administered | |
| 88383125 | 8838312 | Product commingling | |
| 88383125 | 8838312 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 88383125 | 8838312 | 1 | 2007 | 0 |