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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125872031 | 12587203 | 1 | I | 20160523 | 20160607 | 20160725 | 20160725 | EXP | US-ASTELLAS-2016US022315 | ASTELLAS | 16.01 | YR | M | Y | 165.00000 | KG | 20160725 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 125872031 | 12587203 | 1 | PS | TACROLIMUS. | TACROLIMUS | 1 | Topical | 0.1 %, TWICE DAILY | 50777 | .1 | PCT | OINTMENT | BID | ||||||
| 125872031 | 12587203 | 2 | C | ALBUTEROL SULFATE. | ALBUTEROL SULFATE | 1 | Respiratory (inhalation) | 1.25MG/3ML, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
| 125872031 | 12587203 | 3 | C | FLOVENT | FLUTICASONE PROPIONATE | 1 | Respiratory (inhalation) | 220MCG/ACT, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
| 125872031 | 12587203 | 4 | C | PREDNISONE. | PREDNISONE | 1 | Unknown | UNK UNK, UNKNOWN FREQ. | U | 0 | FORMULATION UNKNOWN | ||||||||
| 125872031 | 12587203 | 5 | C | LORATADINE. | LORATADINE | 1 | Oral | U | 0 | 10 | MG | TABLET | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 125872031 | 12587203 | 1 | Dermatitis atopic |
| 125872031 | 12587203 | 2 | Product used for unknown indication |
| 125872031 | 12587203 | 3 | Product used for unknown indication |
| 125872031 | 12587203 | 4 | Product used for unknown indication |
| 125872031 | 12587203 | 5 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 125872031 | 12587203 | OT |
| 125872031 | 12587203 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 125872031 | 12587203 | Blood pressure increased | |
| 125872031 | 12587203 | Off label use | |
| 125872031 | 12587203 | Type 2 diabetes mellitus |
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 |
|---|---|---|---|---|---|---|
| 125872031 | 12587203 | 1 | 20060420 | 20070203 | 0 | |
| 125872031 | 12587203 | 4 | 201604 | 201604 | 0 |