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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126517821 | 12651782 | 1 | I | 200908 | 20090915 | 20160815 | 20160815 | EXP | FR-PFIZER INC-FR-WYE-G04438009 | PFIZER | 40.00 | YR | F | Y | 0.00000 | 20160815 | OT | FR | FR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 126517821 | 12651782 | 1 | PS | ADVIL | IBUPROFEN | 1 | Oral | UNKNOWN | Y | 18989 | TABLET | ||||||||
| 126517821 | 12651782 | 2 | SS | ADVIL | IBUPROFEN | 1 | Y | 18989 | TABLET | ||||||||||
| 126517821 | 12651782 | 3 | SS | XANAX | ALPRAZOLAM | 1 | Oral | UNKNOWN | U | 18276 | TABLET | ||||||||
| 126517821 | 12651782 | 4 | SS | SERESTA | OXAZEPAM | 1 | Oral | UNKNOWN | Y | 0 | |||||||||
| 126517821 | 12651782 | 5 | SS | TEGRETOL | CARBAMAZEPINE | 1 | Oral | UNKNOWN | Y | 0 | |||||||||
| 126517821 | 12651782 | 6 | SS | ZYPREXA | OLANZAPINE | 1 | Oral | UNKNOWN | 0 | ||||||||||
| 126517821 | 12651782 | 7 | SS | AUGMENTIN | AMOXICILLINCLAVULANATE POTASSIUM | 1 | Oral | UNKNOWN | Y | 0 | |||||||||
| 126517821 | 12651782 | 8 | C | DOLIPRANE | ACETAMINOPHEN | 1 | Oral | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 126517821 | 12651782 | 1 | Headache |
| 126517821 | 12651782 | 2 | Odynophagia |
| 126517821 | 12651782 | 4 | Depression |
| 126517821 | 12651782 | 5 | Depression |
| 126517821 | 12651782 | 6 | Depression |
| 126517821 | 12651782 | 7 | Tonsillitis |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 126517821 | 12651782 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 126517821 | 12651782 | Alanine aminotransferase increased | |
| 126517821 | 12651782 | Blood creatine phosphokinase increased | |
| 126517821 | 12651782 | Blood lactate dehydrogenase increased | |
| 126517821 | 12651782 | Drug reaction with eosinophilia and systemic symptoms | |
| 126517821 | 12651782 | Eczema | |
| 126517821 | 12651782 | Eosinophilia | |
| 126517821 | 12651782 | Generalised erythema | |
| 126517821 | 12651782 | Hypotension | |
| 126517821 | 12651782 | Leukocytosis | |
| 126517821 | 12651782 | Myalgia | |
| 126517821 | 12651782 | Rales | |
| 126517821 | 12651782 | Rash vesicular | |
| 126517821 | 12651782 | Skin exfoliation |
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 |
|---|---|---|---|---|---|---|
| 126517821 | 12651782 | 1 | 20090803 | 20090807 | 0 | |
| 126517821 | 12651782 | 3 | 200803 | 20090730 | 0 | |
| 126517821 | 12651782 | 4 | 20090730 | 20090821 | 0 | |
| 126517821 | 12651782 | 5 | 20090730 | 20090821 | 0 | |
| 126517821 | 12651782 | 6 | 200803 | 20090730 | 0 | |
| 126517821 | 12651782 | 7 | 20090807 | 20090810 | 0 | |
| 126517821 | 12651782 | 8 | 20090807 | 0 |