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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123280194 | 12328019 | 4 | F | 201601 | 20160629 | 20160503 | 20160711 | EXP | PHEH2016US009997 | NOVARTIS | 74.37 | YR | F | Y | 73.30000 | KG | 20160711 | OT | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 123280194 | 12328019 | 1 | PS | LETROZOLE. | LETROZOLE | 1 | Unknown | 2.5 MG, UNK | U | 20726 | 2.5 | MG | |||||||
| 123280194 | 12328019 | 2 | SS | ANASTROZOLE. | ANASTROZOLE | 1 | Unknown | 1 MG, UNK | U | 0 | 1 | MG | |||||||
| 123280194 | 12328019 | 3 | SS | AROMASIN | EXEMESTANE | 1 | Unknown | 45 MG, QD (ONCE AT NIGHT FOR 1 MONTH) | 0 | 45 | MG | TABLET | QD | ||||||
| 123280194 | 12328019 | 4 | SS | AROMASIN | EXEMESTANE | 1 | Unknown | UNK | 0 | TABLET | |||||||||
| 123280194 | 12328019 | 5 | C | HCTZ | HYDROCHLOROTHIAZIDE | 1 | Unknown | 12.5 MG, UNK | U | 0 | 12.5 | MG | |||||||
| 123280194 | 12328019 | 6 | C | EDARBI | AZILSARTAN KAMEDOXOMIL | 1 | Unknown | 40 MG, QD (DAILY IN MORNING) | 0 | 40 | MG | QD | |||||||
| 123280194 | 12328019 | 7 | C | AMLODIPINE | AMLODIPINE BESYLATE | 1 | Unknown | 10 MG, QD | 0 | 10 | MG | QD |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 123280194 | 12328019 | 1 | Product used for unknown indication |
| 123280194 | 12328019 | 2 | Product used for unknown indication |
| 123280194 | 12328019 | 3 | Product used for unknown indication |
| 123280194 | 12328019 | 5 | Product used for unknown indication |
| 123280194 | 12328019 | 6 | Blood pressure measurement |
| 123280194 | 12328019 | 7 | Blood pressure measurement |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 123280194 | 12328019 | HO |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 123280194 | 12328019 | Alopecia | |
| 123280194 | 12328019 | Amnesia | |
| 123280194 | 12328019 | Arthritis | |
| 123280194 | 12328019 | Asthenia | |
| 123280194 | 12328019 | Back pain | |
| 123280194 | 12328019 | Confusional state | |
| 123280194 | 12328019 | Depressed mood | |
| 123280194 | 12328019 | Eye disorder | |
| 123280194 | 12328019 | Feeling abnormal | |
| 123280194 | 12328019 | Gait disturbance | |
| 123280194 | 12328019 | Injury | |
| 123280194 | 12328019 | Joint swelling | |
| 123280194 | 12328019 | Limb injury | |
| 123280194 | 12328019 | Malaise | |
| 123280194 | 12328019 | Peripheral swelling | |
| 123280194 | 12328019 | Visual impairment | |
| 123280194 | 12328019 | 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 |
|---|---|---|---|---|---|---|
| 123280194 | 12328019 | 3 | 20160301 | 0 |