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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126894641 | 12689464 | 1 | I | 20160810 | 20160826 | 20160826 | PER | US-GLAXOSMITHKLINE-US2016116239 | GLAXOSMITHKLINE | 0.00 | F | Y | 0.00000 | 20160826 | CN | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126894641 | 12689464 | 1 | PS | FLOVENT DISKUS | FLUTICASONE PROPIONATE | 1 | 1 PUFF(S), PRN | U | U | UNKNOWN | 21433 | 1 | DF | ||||||
126894641 | 12689464 | 2 | SS | TANZEUM | ALBIGLUTIDE | 1 | 30 MG, UNK | U | U | GAOH17BDB | 0 | 30 | MG | SOLUTION FOR INJECTION IN PRE-FILLED PEN | |||||
126894641 | 12689464 | 3 | C | HYDROCHLOROTHIAZIDE. | HYDROCHLOROTHIAZIDE | 1 | 0 | ||||||||||||
126894641 | 12689464 | 4 | C | LEVEMIR | INSULIN DETEMIR | 1 | 0 | ||||||||||||
126894641 | 12689464 | 5 | C | LOSARTAN. | LOSARTAN | 1 | 0 | ||||||||||||
126894641 | 12689464 | 6 | C | NOVOLOG | INSULIN ASPART | 1 | 0 | ||||||||||||
126894641 | 12689464 | 7 | C | POTASSIUM | POTASSIUM | 1 | 0 | ||||||||||||
126894641 | 12689464 | 8 | C | PRAVACHOL | PRAVASTATIN SODIUM | 1 | 0 | ||||||||||||
126894641 | 12689464 | 9 | C | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | 0 | ||||||||||||
126894641 | 12689464 | 10 | C | VITAMIN D | CHOLECALCIFEROL | 1 | 0 | ||||||||||||
126894641 | 12689464 | 11 | C | XOPENEX | LEVALBUTEROL HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126894641 | 12689464 | 2 | Product used for unknown indication |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126894641 | 12689464 | Abdominal pain upper | |
126894641 | 12689464 | Accidental exposure to product | |
126894641 | 12689464 | Intentional product misuse | |
126894641 | 12689464 | Product quality issue | |
126894641 | 12689464 | Treatment noncompliance | |
126894641 | 12689464 | Underdose |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |