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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126233081 | 12623308 | 1 | I | 20160726 | 20160804 | 20160804 | EXP | US-SA-2016SA137793 | AVENTIS | 82.00 | YR | E | F | Y | 0.00000 | 20160804 | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126233081 | 12623308 | 1 | PS | LANTUS SOLOSTAR | INSULIN GLARGINE | 1 | Unknown | DOSE:38 UNIT(S) | UNK | 21081 | QD | ||||||||
126233081 | 12623308 | 2 | C | SOLOSTAR | DEVICE | 1 | 0 | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126233081 | 12623308 | 1 | Type 2 diabetes mellitus |
126233081 | 12623308 | 2 | Type 2 diabetes mellitus |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126233081 | 12623308 | DS |
126233081 | 12623308 | HO |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126233081 | 12623308 | Blood glucose abnormal | |
126233081 | 12623308 | Condition aggravated | |
126233081 | 12623308 | Hydronephrosis | |
126233081 | 12623308 | Macular degeneration | |
126233081 | 12623308 | Nephrolithiasis | |
126233081 | 12623308 | Sepsis | |
126233081 | 12623308 | Septic shock | |
126233081 | 12623308 | Urethral obstruction | |
126233081 | 12623308 | Visual impairment |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |