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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98808495 | 9880849 | 5 | F | 20160826 | 20140207 | 20160829 | EXP | US-PFIZER INC-2014035306 | PFIZER | 0.00 | F | Y | 0.00000 | 20160829 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
98808495 | 9880849 | 1 | PS | LYRICA | PREGABALIN | 1 | 600 MG, DAILY (TWO IN THE MORNING, TWO IN THE AFTERNOON AND TWO IN THE EVENING) | 21446 | 600 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
98808495 | 9880849 | 1 | Fibromyalgia |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
98808495 | 9880849 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
98808495 | 9880849 | Condition aggravated | |
98808495 | 9880849 | Feeling abnormal | |
98808495 | 9880849 | Headache | |
98808495 | 9880849 | Malaise | |
98808495 | 9880849 | Mobility decreased | |
98808495 | 9880849 | Stress | |
98808495 | 9880849 | Systemic lupus erythematosus | |
98808495 | 9880849 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |