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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127562541 | 12756254 | 1 | I | 20160907 | 20160907 | 20160916 | 20160916 | PER | US-TEVA-691572USA | TEVA | 0.00 | M | Y | 0.00000 | 20160917 | CN | COUNTRY NOT SPECIFIED | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127562541 | 12756254 | 1 | PS | PROAIR HFA | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | U | DAC33A | 21457 | INHALATION VAPOUR | ||||||||
127562541 | 12756254 | 2 | C | ALLERGY MEDICATION | DIPHENHYDRAMINE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
no results found |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127562541 | 12756254 | Device malfunction | |
127562541 | 12756254 | Drug ineffective | |
127562541 | 12756254 | Dyspnoea | |
127562541 | 12756254 | Feeling hot | |
127562541 | 12756254 | Gallbladder disorder |
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 |
---|---|---|---|---|---|---|
127562541 | 12756254 | 1 | 2013 | 0 |