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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113714803 | 11371480 | 3 | F | 20130227 | 20160726 | 20150812 | 20160728 | PER | PHEH2013US005059 | NOVARTIS | 36.63 | YR | M | Y | 0.00000 | 20160728 | CN | COUNTRY NOT SPECIFIED | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 113714803 | 11371480 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 5 MG, QD | Y | F0014 | 22334 | 5 | MG | TABLET | QD | ||||
| 113714803 | 11371480 | 2 | SS | AFINITOR | EVEROLIMUS | 1 | Y | 22334 | TABLET | ||||||||||
| 113714803 | 11371480 | 3 | C | SODIUM BICARBONATE. | SODIUM BICARBONATE | 1 | Unknown | 300 MG IN THE MORNING AND 300 MG AT NIGHT | 0 | 600 | MG | TABLET | |||||||
| 113714803 | 11371480 | 4 | C | AMLODIPIN | AMLODIPINE BESYLATE | 1 | Unknown | U | 0 | ||||||||||
| 113714803 | 11371480 | 5 | C | LOSARTAN. | LOSARTAN | 1 | Unknown | 10 MG, UNK | 0 | 10 | MG | ||||||||
| 113714803 | 11371480 | 6 | C | LOSARTAN. | LOSARTAN | 1 | Unknown | 25 MG, UNK | 0 | 25 | MG | ||||||||
| 113714803 | 11371480 | 7 | C | MULTI VITAMIN | VITAMINS | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 113714803 | 11371480 | 1 | Angiomyolipoma |
| 113714803 | 11371480 | 2 | Benign neoplasm |
| 113714803 | 11371480 | 3 | Blood uric acid increased |
| 113714803 | 11371480 | 4 | Hypertension |
| 113714803 | 11371480 | 5 | Hypertension |
| 113714803 | 11371480 | 7 | Product used for unknown indication |
Outcome of event
| no results found |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 113714803 | 11371480 | Accident at work | |
| 113714803 | 11371480 | Acne | |
| 113714803 | 11371480 | Aphthous ulcer | |
| 113714803 | 11371480 | Blood pressure increased | |
| 113714803 | 11371480 | Dizziness | |
| 113714803 | 11371480 | Fatigue | |
| 113714803 | 11371480 | Furuncle | |
| 113714803 | 11371480 | Gastroenteritis viral | |
| 113714803 | 11371480 | Impaired healing | |
| 113714803 | 11371480 | Joint injury | |
| 113714803 | 11371480 | Joint swelling | |
| 113714803 | 11371480 | Neoplasm | |
| 113714803 | 11371480 | Oral pain | |
| 113714803 | 11371480 | Pruritus | |
| 113714803 | 11371480 | Scratch | |
| 113714803 | 11371480 | 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 |
|---|---|---|---|---|---|---|
| 113714803 | 11371480 | 1 | 20130227 | 20160711 | 0 |