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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
89287262 | 8928726 | 2 | F | 2012 | 20121115 | 20121128 | 20130702 | EXP | US-PFIZER INC-2012294086 | PFIZER | 29.00 | YR | M | Y | 0.00000 | 20130702 | OT | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
89287262 | 8928726 | 1 | PS | IBUPROFEN | 1 | UNKNOWN | UNK | D | 18989 | ||||||||||
89287262 | 8928726 | 2 | SS | IBUPROFEN | 1 | D | 18989 | ||||||||||||
89287262 | 8928726 | 3 | SS | TYLENOL | 1 | UNKNOWN | UNK | D | 0 | ||||||||||
89287262 | 8928726 | 4 | SS | TYLENOL | 1 | D | 0 | ||||||||||||
89287262 | 8928726 | 5 | SS | REBIF | 1 | SUBCUTANEOUS | 3 TIMES PER WEEK | D | AU003961 | 0 | INJECTION | ||||||||
89287262 | 8928726 | 6 | SS | REBIF | 1 | SUBCUTANEOUS | 22 UG, UNK | D | AU003961 | 0 | 22 | UG | INJECTION | ||||||
89287262 | 8928726 | 7 | SS | ALEVE | 1 | UNKNOWN | D | 0 | |||||||||||
89287262 | 8928726 | 8 | SS | ALEVE | 1 | D | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
89287262 | 8928726 | 1 | Headache |
89287262 | 8928726 | 2 | Premedication |
89287262 | 8928726 | 3 | Headache |
89287262 | 8928726 | 4 | Premedication |
89287262 | 8928726 | 5 | Multiple sclerosis |
89287262 | 8928726 | 7 | Headache |
89287262 | 8928726 | 8 | Premedication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
89287262 | 8928726 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
89287262 | 8928726 | Asthenia | |
89287262 | 8928726 | Balance disorder | |
89287262 | 8928726 | Feeling abnormal | |
89287262 | 8928726 | Gait disturbance | |
89287262 | 8928726 | Headache | |
89287262 | 8928726 | Injection site erythema | |
89287262 | 8928726 | Liver function test abnormal | |
89287262 | 8928726 | Malaise | |
89287262 | 8928726 | Memory impairment | |
89287262 | 8928726 | Multiple sclerosis | |
89287262 | 8928726 | Pain in extremity |
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 |
---|---|---|---|---|---|---|
89287262 | 8928726 | 1 | 201204 | 0 | ||
89287262 | 8928726 | 3 | 201204 | 0 | ||
89287262 | 8928726 | 5 | 20110311 | 0 | ||
89287262 | 8928726 | 6 | 201204 | 0 | ||
89287262 | 8928726 | 7 | 201204 | 0 |