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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116622213 | 11662221 | 3 | F | 20151019 | 20160721 | 20151026 | 20160725 | EXP | PHHY2015CA137743 | NOVARTIS | 46.65 | YR | F | Y | 98.00000 | KG | 20160725 | CN | CA | CA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
116622213 | 11662221 | 1 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | 300 MG, BIW | U | 0 | 300 | MG | QOW | ||||||
116622213 | 11662221 | 2 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | UNK | U | S0066B | 0 | ||||||||
116622213 | 11662221 | 3 | SS | XOLAIR | OMALIZUMAB | 1 | Subcutaneous | UNK | U | 0 | |||||||||
116622213 | 11662221 | 4 | PS | ONBREZ BREEZHALER | INDACATEROL | 1 | Respiratory (inhalation) | UNK | U | 22383 | |||||||||
116622213 | 11662221 | 5 | C | SYMBICORT | BUDESONIDEFORMOTEROL FUMARATE DIHYDRATE | 1 | Unknown | UNK | U | 0 | |||||||||
116622213 | 11662221 | 6 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | UNK | U | 0 | |||||||||
116622213 | 11662221 | 7 | C | DEXILANT | DEXLANSOPRAZOLE | 1 | Unknown | UNK | U | 0 | |||||||||
116622213 | 11662221 | 8 | C | CANDESARTAN | CANDESARTAN | 1 | Unknown | UNK | U | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
116622213 | 11662221 | 1 | Asthma |
116622213 | 11662221 | 4 | Product used for unknown indication |
116622213 | 11662221 | 5 | Product used for unknown indication |
116622213 | 11662221 | 6 | Product used for unknown indication |
116622213 | 11662221 | 7 | Product used for unknown indication |
116622213 | 11662221 | 8 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
116622213 | 11662221 | HO |
116622213 | 11662221 | LT |
116622213 | 11662221 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
116622213 | 11662221 | Altered state of consciousness | |
116622213 | 11662221 | Back pain | |
116622213 | 11662221 | Blood pressure increased | |
116622213 | 11662221 | Cough | |
116622213 | 11662221 | Dizziness | |
116622213 | 11662221 | Dysphonia | |
116622213 | 11662221 | Dyspnoea | |
116622213 | 11662221 | Headache | |
116622213 | 11662221 | Pallor | |
116622213 | 11662221 | Sneezing | |
116622213 | 11662221 | Vision blurred | |
116622213 | 11662221 | Wheezing |
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 |
---|---|---|---|---|---|---|
116622213 | 11662221 | 1 | 20151019 | 0 | ||
116622213 | 11662221 | 2 | 20160707 | 0 | ||
116622213 | 11662221 | 3 | 20160721 | 0 |