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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128019251 | 12801925 | 1 | I | 0 | 20160930 | 20160930 | DIR | US-FDA-351956 | FDA-CTU | 54.00 | YR | F | N | 57.15000 | KG | 20160930 | N | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 128019251 | 12801925 | 1 | PS | SYNTHROID | LEVOTHYROXINE SODIUM | 1 | Oral | OTHER ORAL? | Y | D | 0 | ||||||||
| 128019251 | 12801925 | 3 | C | OMEPRAZOLE. | OMEPRAZOLE | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 5 | C | VENTOLIN | ALBUTEROL SULFATE | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 7 | C | FUROSEMIDE. | FUROSEMIDE | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 9 | C | SIMVASTATIN. | SIMVASTATIN | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 10 | SS | SODIUM BICARBONATE. | SODIUM BICARBONATE | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 12 | C | FLUDROCORTISONE | FLUDROCORTISONE | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 14 | C | ALLIPURINOL | 2 | 0 | |||||||||||||
| 128019251 | 12801925 | 16 | C | CALCITROL | CALCITRIOL | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 18 | C | HUMALOG | INSULIN LISPRO | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 20 | C | LANTUS | INSULIN GLARGINE | 1 | 0 | ||||||||||||
| 128019251 | 12801925 | 22 | C | TYLENOL | ACETAMINOPHEN | 1 | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 128019251 | 12801925 | 1 | Thyroid disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 128019251 | 12801925 | DS |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 128019251 | 12801925 | Dyspnoea | |
| 128019251 | 12801925 | Hyperhidrosis | |
| 128019251 | 12801925 | Insomnia | |
| 128019251 | 12801925 | Nausea | |
| 128019251 | 12801925 | Nervousness | |
| 128019251 | 12801925 | Weight increased |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |