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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121406412 | 12140641 | 2 | F | 20160122 | 20160303 | 20160706 | EXP | CA-APOTEX-2015AP015166 | APOTEX | 0.00 | Y | 0.00000 | 20160706 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
121406412 | 12140641 | 1 | PS | APO-SALVENT | ALBUTEROL | 1 | Oral | UNK, TID | U | U | 75717 | TID | |||||||
121406412 | 12140641 | 2 | SS | SALBUTAMOL | ALBUTEROL | 1 | Unknown | UNK | U | U | 0 | AEROSOL (SPRAY AND INHALATION) | |||||||
121406412 | 12140641 | 3 | C | JANUVIA | SITAGLIPTIN PHOSPHATE | 1 | Unknown | UNK | U | U | 0 | TABLET | |||||||
121406412 | 12140641 | 4 | C | METFORMIN | METFORMIN HYDROCHLORIDE | 1 | Unknown | UNK | U | U | 0 | TABLET | |||||||
121406412 | 12140641 | 5 | C | PERINDOPRIL | PERINDOPRIL | 1 | Unknown | UNK | U | U | 0 | ||||||||
121406412 | 12140641 | 6 | C | SPIRIVA | TIOTROPIUM BROMIDE MONOHYDRATE | 1 | Unknown | UNK | U | U | 0 | CAPSULE |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
121406412 | 12140641 | 1 | Chronic obstructive pulmonary disease |
121406412 | 12140641 | 2 | Chronic obstructive pulmonary disease |
121406412 | 12140641 | 3 | Product used for unknown indication |
121406412 | 12140641 | 4 | Product used for unknown indication |
121406412 | 12140641 | 5 | Product used for unknown indication |
121406412 | 12140641 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
121406412 | 12140641 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
121406412 | 12140641 | Device issue | |
121406412 | 12140641 | Drug ineffective | |
121406412 | 12140641 | Nausea | |
121406412 | 12140641 | Product substitution issue | |
121406412 | 12140641 | Vomiting |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |