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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126407282 | 12640728 | 2 | F | 20120404 | 20160822 | 20160810 | 20160824 | EXP | GB-MHRA-EYC 00140033 | GB-LEO PHARMA-243449 | LEO PHARM | 36.00 | YR | M | Y | 73.00000 | KG | 20160824 | CN | GB | GB |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126407282 | 12640728 | 1 | PS | DAIVONEX Ointment | CALCIPOTRIENE | 1 | Y | U | 20273 | OINTMENT | |||||||||
126407282 | 12640728 | 2 | SS | DAIVOBET | BETAMETHASONE DIPROPIONATECALCIPOTRIENE | 1 | Y | U | 21852 | OINTMENT | |||||||||
126407282 | 12640728 | 3 | SS | QUETIAPINE FUMARATE. | QUETIAPINE FUMARATE | 1 | Oral | 38400 | MG | U | 0 | 600 | MG | PROLONGED-RELEASE TABLET | QD | ||||
126407282 | 12640728 | 4 | SS | PINEWOOD LABS KETOPINE | KETOCONAZOLE | 1 | U | U | 0 | OINTMENT | |||||||||
126407282 | 12640728 | 5 | C | VITAMIN D3 | CHOLECALCIFEROL | 1 | 0 | 10000 | IU | QD | |||||||||
126407282 | 12640728 | 6 | C | DAIVOBET | BETAMETHASONE DIPROPIONATECALCIPOTRIENE | 1 | 0 |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126407282 | 12640728 | 1 | Pruritus |
126407282 | 12640728 | 2 | Pruritus |
126407282 | 12640728 | 3 | Bipolar I disorder |
126407282 | 12640728 | 4 | Product used for unknown indication |
126407282 | 12640728 | 5 | Vitamin D deficiency |
126407282 | 12640728 | 6 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126407282 | 12640728 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126407282 | 12640728 | Blood cholesterol increased | |
126407282 | 12640728 | Dermatitis | |
126407282 | 12640728 | Eczema | |
126407282 | 12640728 | Guttate psoriasis | |
126407282 | 12640728 | Product use issue | |
126407282 | 12640728 | Pruritus | |
126407282 | 12640728 | Psoriasis | |
126407282 | 12640728 | Vitamin D decreased |
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 |
---|---|---|---|---|---|---|
126407282 | 12640728 | 3 | 20120201 | 0 | ||
126407282 | 12640728 | 4 | 2012 | 0 | ||
126407282 | 12640728 | 5 | 201511 | 0 |