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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122120075 | 12212007 | 5 | F | 2015 | 20160704 | 20160325 | 20160711 | EXP | PHHY2015BR118326 | NOVARTIS | 0.00 | F | Y | 59.00000 | KG | 20160711 | MD | BR | BR |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 122120075 | 12212007 | 1 | PS | AFINITOR | EVEROLIMUS | 1 | Oral | 1 DF OF 5 MG, QD | Y | SA353/SC606 | 22334 | 5 | MG | TABLET | QD | ||||
| 122120075 | 12212007 | 2 | C | AROMASIN | EXEMESTANE | 1 | Oral | 1 DF, QD | 0 | 1 | DF | TABLET | QD | ||||||
| 122120075 | 12212007 | 3 | C | ZOMETA | ZOLEDRONIC ACID | 1 | Oral | 1 DF, Q3MO | 0 | 1 | DF | AMPOULE | |||||||
| 122120075 | 12212007 | 4 | C | VITAMIN D | CHOLECALCIFEROL | 1 | Oral | 8 DF, QD | 0 | 8 | DF | DROPS | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 122120075 | 12212007 | 1 | Breast cancer metastatic |
| 122120075 | 12212007 | 2 | Breast cancer |
| 122120075 | 12212007 | 3 | Bone disorder |
| 122120075 | 12212007 | 4 | Bone disorder |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 122120075 | 12212007 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 122120075 | 12212007 | Abdominal pain | |
| 122120075 | 12212007 | Acne | |
| 122120075 | 12212007 | Alopecia | |
| 122120075 | 12212007 | Aphthous ulcer | |
| 122120075 | 12212007 | Arthralgia | |
| 122120075 | 12212007 | Blister | |
| 122120075 | 12212007 | Blood cholesterol increased | |
| 122120075 | 12212007 | Bone pain | |
| 122120075 | 12212007 | Cough | |
| 122120075 | 12212007 | Decreased immune responsiveness | |
| 122120075 | 12212007 | Drug ineffective | |
| 122120075 | 12212007 | Dysgeusia | |
| 122120075 | 12212007 | Epistaxis | |
| 122120075 | 12212007 | Influenza | |
| 122120075 | 12212007 | Limb injury | |
| 122120075 | 12212007 | Malaise | |
| 122120075 | 12212007 | Mass | |
| 122120075 | 12212007 | Nasal discomfort | |
| 122120075 | 12212007 | Nasal disorder | |
| 122120075 | 12212007 | Nasal injury | |
| 122120075 | 12212007 | Oropharyngeal discomfort | |
| 122120075 | 12212007 | Pain in extremity | |
| 122120075 | 12212007 | Peripheral swelling | |
| 122120075 | 12212007 | Pruritus | |
| 122120075 | 12212007 | Pyrexia | |
| 122120075 | 12212007 | Saliva altered | |
| 122120075 | 12212007 | Skin atrophy | |
| 122120075 | 12212007 | Skin exfoliation | |
| 122120075 | 12212007 | Stomatitis | |
| 122120075 | 12212007 | Weight decreased | |
| 122120075 | 12212007 | Weight increased |
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 |
|---|---|---|---|---|---|---|
| 122120075 | 12212007 | 1 | 20150813 | 0 | ||
| 122120075 | 12212007 | 2 | 20150818 | 0 | ||
| 122120075 | 12212007 | 3 | 2015 | 0 |