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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127427951 | 12742795 | 1 | I | 20160704 | 20160907 | 20160914 | 20160914 | EXP | CN-PFIZER INC-2016425036 | PFIZER | 28.00 | YR | F | Y | 52.00000 | KG | 20160914 | OT | CN | CN |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127427951 | 12742795 | 1 | PS | ZITHROMAX | AZITHROMYCIN DIHYDRATE | 1 | Oral | 500 MG, 1X/DAY | Y | 20130521 | 50784 | 500 | MG | FILM-COATED TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127427951 | 12742795 | 1 | Lung infection |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
127427951 | 12742795 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127427951 | 12742795 | Abdominal pain | |
127427951 | 12742795 | Diarrhoea | |
127427951 | 12742795 | Gastrointestinal pain |
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 |
---|---|---|---|---|---|---|
127427951 | 12742795 | 1 | 20160704 | 20160705 | 0 |