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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127129331 | 12712933 | 1 | I | 20150818 | 20160902 | 20160902 | PER | US-APOTEX-2015AP012378 | APOTEX | IAMMATTEO, M; BLUMENTHAL, KG; SAFF, R; LONG, AA; BANERJI, A.. SAFETY AND OUTCOMES OF TEST DOSES FOR THE EVALUATION OF ADVERSE DRUG REACTIONS: A 5-YEAR RETROSPECTIVE REVIEW. J-ALLERGY-CLIN-IMMUNOL-PRACT. 2014;2(6):768-774 | 45.00 | YR | F | Y | 0.00000 | 20160902 | MD | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127129331 | 12712933 | 1 | PS | AZITHROMYCIN ANHYDROUS. | AZITHROMYCIN ANHYDROUS | 1 | Unknown | 65507 | TABLET |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127129331 | 12712933 | 1 | Allergy test |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127129331 | 12712933 | Chills | |
127129331 | 12712933 | Dry throat | |
127129331 | 12712933 | Nausea |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |