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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123966132 | 12396613 | 2 | F | 20160701 | 20160524 | 20160711 | EXP | US-SHIRE-US201606210 | SHIRE | 0.00 | F | Y | 70.75000 | KG | 20160711 | MD | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123966132 | 12396613 | 1 | PS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | 40 MG, UNKNOWN | Y | 21977 | 40 | MG | CAPSULE | |||||||
| 123966132 | 12396613 | 2 | SS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 30 MG, UNKNOWN | Y | 21977 | 30 | MG | CAPSULE | ||||||
| 123966132 | 12396613 | 3 | SS | VYVANSE | LISDEXAMFETAMINE DIMESYLATE | 1 | Oral | 20 MG, UNKNOWN | Y | 21977 | 20 | MG | CAPSULE | ||||||
| 123966132 | 12396613 | 4 | C | PRISTIQ EXTENDED-RELEASE | DESVENLAFAXINE SUCCINATE | 1 | Unknown | 100 MG, UNKNOWN | 0 | 100 | MG | ||||||||
| 123966132 | 12396613 | 5 | C | ATENOLOL. | ATENOLOL | 1 | Unknown | 50 MG, UNKNOWN | 0 | 50 | MG | ||||||||
| 123966132 | 12396613 | 6 | C | DEPLIN | LEVOMEFOLATE CALCIUM | 1 | Unknown | 15 MG, UNKNOWN | 0 | 15 | MG | ||||||||
| 123966132 | 12396613 | 7 | C | MINASTRIN 24 FE | ETHINYL ESTRADIOLNORETHINDRONE ACETATE | 1 | Unknown | 24 MG, 1X/DAY:QD | 0 | 24 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123966132 | 12396613 | 1 | Major depression |
| 123966132 | 12396613 | 4 | Depression |
| 123966132 | 12396613 | 5 | Hypertension |
| 123966132 | 12396613 | 6 | Product used for unknown indication |
| 123966132 | 12396613 | 7 | Contraception |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123966132 | 12396613 | OT |
| 123966132 | 12396613 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123966132 | 12396613 | Chromaturia | |
| 123966132 | 12396613 | Myalgia | |
| 123966132 | 12396613 | Peripheral swelling | |
| 123966132 | 12396613 | Product use issue | |
| 123966132 | 12396613 | Renal failure | |
| 123966132 | 12396613 | Rhabdomyolysis | |
| 123966132 | 12396613 | Wrong technique in product usage process |
Reporting Sources (this data is often not reported and may therefore be missing here)
| no results found |
Therapies reported
| no results found |