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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127558321 | 12755832 | 1 | I | 201512 | 20160531 | 20160916 | 20160916 | PER | US-ASTRAZENECA-2016SE58925 | ASTRAZENECA | 865.00 | MON | F | Y | 81.20000 | KG | 20160916 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
127558321 | 12755832 | 1 | PS | BYDUREON | EXENATIDE | 1 | Subcutaneous | 24 | MG | FN0142 | 22200 | 2 | MG | /wk | |||||
127558321 | 12755832 | 2 | SS | BYETTA | EXENATIDE | 1 | Unknown | 5 | U | 0 | SOLUTION FOR INJECTION IN PRE-FILLED PEN | ||||||||
127558321 | 12755832 | 3 | SS | BYETTA | EXENATIDE | 1 | Unknown | 10 | U | 0 | SOLUTION FOR INJECTION IN PRE-FILLED PEN | ||||||||
127558321 | 12755832 | 4 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | U | U | 0 | 10 | MG | TABLET | QD | |||||
127558321 | 12755832 | 5 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | U | U | 0 | 20 | MG | TABLET | QD | |||||
127558321 | 12755832 | 6 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | U | U | 0 | 40 | MG | TABLET | QD | |||||
127558321 | 12755832 | 7 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | U | U | 0 | 40 | MG | TABLET | QD | |||||
127558321 | 12755832 | 8 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | U | U | 0 | 20 | MG | TABLET | QD | |||||
127558321 | 12755832 | 9 | SS | LISINOPRIL. | LISINOPRIL | 1 | Oral | U | U | 0 | 20 | MG | TABLET | QD | |||||
127558321 | 12755832 | 10 | SS | METFORMIN HCL | METFORMIN HYDROCHLORIDE | 1 | Oral | 750 MG, NON-AZ PRODUCT | 0 | ||||||||||
127558321 | 12755832 | 11 | C | IMODIUM | LOPERAMIDE HYDROCHLORIDE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
127558321 | 12755832 | 1 | Type 2 diabetes mellitus |
127558321 | 12755832 | 2 | Type 2 diabetes mellitus |
127558321 | 12755832 | 3 | Type 2 diabetes mellitus |
127558321 | 12755832 | 4 | Renal disorder |
127558321 | 12755832 | 5 | Renal disorder |
127558321 | 12755832 | 6 | Renal disorder |
127558321 | 12755832 | 7 | Renal disorder |
127558321 | 12755832 | 8 | Renal disorder |
127558321 | 12755832 | 9 | Renal disorder |
127558321 | 12755832 | 10 | Type 2 diabetes mellitus |
127558321 | 12755832 | 11 | Diarrhoea |
Outcome of event
no results found |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
127558321 | 12755832 | Blood creatinine increased | |
127558321 | 12755832 | Blood glucose increased | |
127558321 | 12755832 | Circumstance or information capable of leading to medication error | |
127558321 | 12755832 | Cold sweat | |
127558321 | 12755832 | Device difficult to use | |
127558321 | 12755832 | Device malfunction | |
127558321 | 12755832 | Diabetes mellitus | |
127558321 | 12755832 | Diarrhoea | |
127558321 | 12755832 | Drug hypersensitivity | |
127558321 | 12755832 | Fall | |
127558321 | 12755832 | Feeling abnormal | |
127558321 | 12755832 | Feeling jittery | |
127558321 | 12755832 | Hypertension | |
127558321 | 12755832 | Nausea | |
127558321 | 12755832 | Pharyngeal disorder | |
127558321 | 12755832 | Underdose | |
127558321 | 12755832 | Vertigo |
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 |
---|---|---|---|---|---|---|
127558321 | 12755832 | 1 | 20160310 | 0 | ||
127558321 | 12755832 | 7 | 201512 | 20160514 | 0 | |
127558321 | 12755832 | 8 | 20160515 | 20160520 | 0 | |
127558321 | 12755832 | 9 | 20160521 | 0 |