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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127365862 | 12736586 | 2 | F | 20160905 | 20160913 | 20160913 | EXP | PHHY2015BR081758 | SANDOZ | 0.00 | F | Y | 51.90000 | KG | 20160913 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127365862 | 12736586 | 1 | SS | EXJADE | DEFERASIROX | 1 | Oral | 2000 MG, QD | 0 | 2000 | MG | DISPERSIBLE TABLET | QD | ||||||
| 127365862 | 12736586 | 2 | SS | EXJADE | DEFERASIROX | 1 | Oral | 5 DF (45 MG/KG), QD | 0 | 45 | MG/KG | DISPERSIBLE TABLET | QD | ||||||
| 127365862 | 12736586 | 3 | PS | OMEPRAZOLE. | OMEPRAZOLE | 1 | Unknown | U | 76515 | ||||||||||
| 127365862 | 12736586 | 4 | SS | FUROSEMIDE. | FUROSEMIDE | 1 | Unknown | U | 0 | ||||||||||
| 127365862 | 12736586 | 5 | SS | DIPYRONE | DIPYRONE | 1 | Unknown | U | 0 | ||||||||||
| 127365862 | 12736586 | 6 | SS | CAPTOPRIL. | CAPTOPRIL | 1 | Unknown | U | 0 | ||||||||||
| 127365862 | 12736586 | 7 | SS | CLONAZEPAM. | CLONAZEPAM | 1 | Unknown | U | 0 | ||||||||||
| 127365862 | 12736586 | 8 | SS | SIMETHICONE (DIMETHICONE) | DIMETHICONE | 1 | Unknown | U | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127365862 | 12736586 | 1 | Thalassaemia beta |
| 127365862 | 12736586 | 3 | Product used for unknown indication |
| 127365862 | 12736586 | 4 | Product used for unknown indication |
| 127365862 | 12736586 | 5 | Product used for unknown indication |
| 127365862 | 12736586 | 6 | Product used for unknown indication |
| 127365862 | 12736586 | 7 | Product used for unknown indication |
| 127365862 | 12736586 | 8 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127365862 | 12736586 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127365862 | 12736586 | Abdominal pain upper | |
| 127365862 | 12736586 | Chikungunya virus infection | |
| 127365862 | 12736586 | Dyspepsia | |
| 127365862 | 12736586 | Fatigue | |
| 127365862 | 12736586 | Myocardial infarction | |
| 127365862 | 12736586 | Nausea | |
| 127365862 | 12736586 | Pain | |
| 127365862 | 12736586 | Serum ferritin increased | |
| 127365862 | 12736586 | Sleep disorder due to a general medical condition |
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 |
|---|---|---|---|---|---|---|
| 127365862 | 12736586 | 1 | 2013 | 0 |