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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127911571 | 12791157 | 1 | I | 20160922 | 20160929 | 20160929 | PER | US-009507513-1609USA011672 | MERCK | 0.00 | F | Y | 0.00000 | 20160929 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127911571 | 12791157 | 1 | PS | PROVENTIL | ALBUTEROL | 1 | Respiratory (inhalation) | 2 INHALATIONS EVERY 12 HOURS, ORAL INHALATION | 160158 | 20503 | 2 | DF | INHALATION POWDER | Q12H | |||||
127911571 | 12791157 | 2 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127911571 | 12791157 | 1 | Chronic obstructive pulmonary disease |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127911571 | 12791157 | Dyspnoea | |
127911571 | 12791157 | Inappropriate schedule of drug administration | |
127911571 | 12791157 | Product quality issue |
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 |
---|---|---|---|---|---|---|
127911571 | 12791157 | 1 | 2014 | 0 |