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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126804561 | 12680456 | 1 | I | 20160812 | 20160824 | 20160824 | EXP | SA-IMPAX LABORATORIES, INC-2016-IPXL-00916 | IMPAX | 50.00 | YR | F | Y | 104.00000 | KG | 20160824 | OT | SA | SA |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
126804561 | 12680456 | 1 | PS | GRANISETRON HYDROCHLORIDE. | GRANISETRON HYDROCHLORIDE | 1 | Intravenous (not otherwise specified) | 1 MG, UNK | U | 78260 | TABLET | ||||||||
126804561 | 12680456 | 2 | SS | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Unknown | 80 MG, UNK | 0 | ||||||||||
126804561 | 12680456 | 3 | SS | PROPRANOLOL | PROPRANOLOLPROPRANOLOL HYDROCHLORIDE | 1 | Unknown | 40 MG, UNK | 0 | ||||||||||
126804561 | 12680456 | 4 | SS | SULPIRIDE | SULPIRIDE | 1 | Unknown | 100 MG, UNK | 0 | 100 | MG | ||||||||
126804561 | 12680456 | 5 | C | METHIMAZOLE. | METHIMAZOLE | 1 | Unknown | 30 MG, UNK | 0 | ||||||||||
126804561 | 12680456 | 6 | C | METHIMAZOLE. | METHIMAZOLE | 1 | Unknown | 15 MG, UNK | 0 | ||||||||||
126804561 | 12680456 | 7 | C | RISPERIDONE. | RISPERIDONE | 1 | Unknown | 4 MG, UNK | 0 | 4 | MG |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
126804561 | 12680456 | 1 | Prophylaxis of nausea and vomiting |
126804561 | 12680456 | 2 | Product used for unknown indication |
126804561 | 12680456 | 4 | Psychotic disorder |
126804561 | 12680456 | 5 | Product used for unknown indication |
126804561 | 12680456 | 7 | Product used for unknown indication |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
126804561 | 12680456 | HO |
126804561 | 12680456 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
126804561 | 12680456 | Cardiac arrest | |
126804561 | 12680456 | Long QT syndrome | |
126804561 | 12680456 | Sinus bradycardia |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |