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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125594821 | 12559482 | 1 | I | 20160617 | 20160715 | 20160715 | PER | US-PFIZER INC-2016310943 | PFIZER | 70.00 | YR | F | Y | 0.00000 | 20160715 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125594821 | 12559482 | 1 | PS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | UNK | U | 50711 | FILM-COATED TABLET | |||||||||
| 125594821 | 12559482 | 2 | SS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | U | 50711 | FILM-COATED TABLET | ||||||||||
| 125594821 | 12559482 | 3 | SS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | U | 50711 | FILM-COATED TABLET | ||||||||||
| 125594821 | 12559482 | 4 | SS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | U | 50711 | FILM-COATED TABLET | ||||||||||
| 125594821 | 12559482 | 5 | SS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | U | 50711 | FILM-COATED TABLET | ||||||||||
| 125594821 | 12559482 | 6 | C | ENBREL | ETANERCEPT | 1 | Subcutaneous | 50 MG, WEEKLY | 0 | 50 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | /wk | ||||||
| 125594821 | 12559482 | 7 | C | CALCIUM | CALCIUM | 1 | UNK | 0 | |||||||||||
| 125594821 | 12559482 | 8 | C | VITAMIN C | ASCORBIC ACID | 1 | UNK | 0 | |||||||||||
| 125594821 | 12559482 | 9 | C | MAGNESIUM | MAGNESIUM | 1 | UNK | 0 | |||||||||||
| 125594821 | 12559482 | 10 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | UNK | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125594821 | 12559482 | 1 | Pyrexia |
| 125594821 | 12559482 | 2 | Nasal congestion |
| 125594821 | 12559482 | 3 | Malaise |
| 125594821 | 12559482 | 4 | White blood cell count increased |
| 125594821 | 12559482 | 5 | Pain |
| 125594821 | 12559482 | 6 | Rheumatoid arthritis |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125594821 | 12559482 | Drug ineffective |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |