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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116587645 | 11658764 | 5 | F | 201410 | 20160812 | 20151026 | 20160817 | PER | PHEH2014US022529 | NOVARTIS | 29.57 | YR | F | Y | 152.00000 | KG | 20160817 | CN | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 116587645 | 11658764 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 10 MG, QD | U | 22334 | 10 | MG | TABLET | QD | |||||
| 116587645 | 11658764 | 2 | SS | AFINITOR | EVEROLIMUS | 1 | Oral | 10 MG, QD | U | 22334 | 10 | MG | TABLET | QD | |||||
| 116587645 | 11658764 | 3 | C | FLOVENT | FLUTICASONE PROPIONATE | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 4 | C | AZELASTINE | AZELASTINE | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 5 | C | FLUTICASONE PROPIONATE. | FLUTICASONE PROPIONATE | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 6 | C | NEXIUM I.V. | ESOMEPRAZOLE SODIUM | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 7 | C | ALLEGRA | FEXOFENADINE HYDROCHLORIDE | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 8 | C | PROAIR HFA | ALBUTEROL SULFATE | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 9 | C | SPRINTEC | ETHINYL ESTRADIOLNORGESTIMATE | 1 | Unknown | U | 0 | ||||||||||
| 116587645 | 11658764 | 10 | C | SINGULAIR | MONTELUKAST SODIUM | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 116587645 | 11658764 | 1 | Angiomyolipoma |
| 116587645 | 11658764 | 3 | Product used for unknown indication |
| 116587645 | 11658764 | 4 | Product used for unknown indication |
| 116587645 | 11658764 | 5 | Product used for unknown indication |
| 116587645 | 11658764 | 6 | Product used for unknown indication |
| 116587645 | 11658764 | 7 | Product used for unknown indication |
| 116587645 | 11658764 | 8 | Product used for unknown indication |
| 116587645 | 11658764 | 9 | Contraception |
| 116587645 | 11658764 | 10 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 116587645 | 11658764 | Aphthous ulcer | |
| 116587645 | 11658764 | Blood iron decreased | |
| 116587645 | 11658764 | Eating disorder | |
| 116587645 | 11658764 | Mouth ulceration | |
| 116587645 | 11658764 | Oral pain | |
| 116587645 | 11658764 | Stomatitis |
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 |
|---|---|---|---|---|---|---|
| 116587645 | 11658764 | 1 | 201409 | 0 | ||
| 116587645 | 11658764 | 2 | 20141106 | 0 |