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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127439363 | 12743936 | 3 | F | 20160620 | 20160912 | 20160914 | 20160920 | EXP | IT-MINISAL02-372978 | IT-MYLANLABS-2016M1037699 | MYLAN | 0.00 | Y | 0.00000 | 20160920 | MD | IT | IT |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 127439363 | 12743936 | 1 | PS | RAMIPRIL. | RAMIPRIL | 1 | Oral | 2.5 MG, QD | 90650 | 2.5 | MG | QD | |||||||
| 127439363 | 12743936 | 2 | SS | NILOTINIB | NILOTINIB | 1 | Oral | 600 MG DAILY | 12600 | MG | Y | U | 0 | 600 | MG | QD | |||
| 127439363 | 12743936 | 3 | SS | NILOTINIB | NILOTINIB | 1 | UNK | 12600 | MG | Y | U | 0 | |||||||
| 127439363 | 12743936 | 4 | SS | NILOTINIB | NILOTINIB | 1 | Oral | 300 MG, UNK | 12600 | MG | Y | U | 0 | 300 | MG | QD | |||
| 127439363 | 12743936 | 5 | SS | NILOTINIB | NILOTINIB | 1 | Oral | 600 MG, QD | 12600 | MG | Y | U | 0 | 600 | MG | QD | |||
| 127439363 | 12743936 | 6 | SS | NILOTINIB | NILOTINIB | 1 | Oral | 300 MG, QD | 12600 | MG | Y | U | 0 | 300 | MG | QD | |||
| 127439363 | 12743936 | 7 | SS | NILOTINIB | NILOTINIB | 1 | Oral | 600 UNK, UNK | 12600 | MG | Y | U | 0 | 600 | MG | QD | |||
| 127439363 | 12743936 | 8 | C | EUTIROX | LEVOTHYROXINE SODIUM | 1 | UNK | D | 0 | ||||||||||
| 127439363 | 12743936 | 9 | C | SENNA /00142201/ | SENNA LEAF | 1 | UNK | D | 0 | ||||||||||
| 127439363 | 12743936 | 10 | C | NEXIUM | ESOMEPRAZOLE MAGNESIUM | 1 | UNK | D | 0 | GASTRO-RESISTANT TABLET | |||||||||
| 127439363 | 12743936 | 11 | C | MOVICOL | POLYETHYLENE GLYCOL 3350POTASSIUM CHLORIDESODIUM BICARBONATESODIUM CHLORIDE | 1 | UNK | D | 0 |
Indications of drugs used
| Event ID | CASEID | INDI DRUG SEQ | INDI PT |
|---|---|---|---|
| 127439363 | 12743936 | 1 | Hypertension |
| 127439363 | 12743936 | 2 | Chronic myeloid leukaemia |
| 127439363 | 12743936 | 8 | Product used for unknown indication |
| 127439363 | 12743936 | 9 | Product used for unknown indication |
| 127439363 | 12743936 | 10 | Product used for unknown indication |
| 127439363 | 12743936 | 11 | Product used for unknown indication |
Outcome of event
| Event ID | CASEID | OUTC COD |
|---|---|---|
| 127439363 | 12743936 | HO |
| 127439363 | 12743936 | OT |
Reactions reported
| Event ID | CASEID | DRUG REC ACT | PT |
|---|---|---|---|
| 127439363 | 12743936 | Abdominal pain upper | |
| 127439363 | 12743936 | Constipation | |
| 127439363 | 12743936 | Gastritis | |
| 127439363 | 12743936 | Hyperhidrosis | |
| 127439363 | 12743936 | Loss of consciousness | |
| 127439363 | 12743936 | Malaise | |
| 127439363 | 12743936 | Nausea | |
| 127439363 | 12743936 | Syncope | |
| 127439363 | 12743936 | Vomiting |
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 |
|---|---|---|---|---|---|---|
| 127439363 | 12743936 | 1 | 201511 | 0 | ||
| 127439363 | 12743936 | 2 | 20150212 | 20150304 | 0 | |
| 127439363 | 12743936 | 3 | 20150311 | 20160715 | 0 | |
| 127439363 | 12743936 | 4 | 20160724 | 20160725 | 0 | |
| 127439363 | 12743936 | 5 | 20160805 | 20160806 | 0 | |
| 127439363 | 12743936 | 6 | 20160812 | 20160813 | 0 | |
| 127439363 | 12743936 | 7 | 20160814 | 0 | ||
| 127439363 | 12743936 | 8 | 1995 | 0 | ||
| 127439363 | 12743936 | 9 | 20151117 | 0 | ||
| 127439363 | 12743936 | 10 | 20150212 | 0 | ||
| 127439363 | 12743936 | 11 | 20151117 | 0 |