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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127263891 | 12726389 | 1 | I | 20160115 | 0 | 20160908 | 20160908 | DIR | FDA-CTU | 19.81 | YR | F | N | 49.94000 | KG | 20160906 | Y | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127263891 | 12726389 | 1 | PS | IMPLANON | ETONOGESTREL | 1 | 0 | ||||||||||||
| 127263891 | 12726389 | 2 | C | ADDERALL | AMPHETAMINE ASPARTATEAMPHETAMINE SULFATEDEXTROAMPHETAMINE SACCHARATEDEXTROAMPHETAMINE SULFATE | 1 | 0 | ||||||||||||
| 127263891 | 12726389 | 3 | C | INSULIN (LLEVEMIER, HUMALOG) | 2 | 0 |
Indications of drugs used
| no results found |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127263891 | 12726389 | DS |
| 127263891 | 12726389 | RI |
| 127263891 | 12726389 | LT |
| 127263891 | 12726389 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127263891 | 12726389 | Blood glucose increased | |
| 127263891 | 12726389 | Malaise | |
| 127263891 | 12726389 | Pollakiuria | |
| 127263891 | 12726389 | Thirst | |
| 127263891 | 12726389 | Type 1 diabetes mellitus | |
| 127263891 | 12726389 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |