The Safety Rates Drug Report

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Drug     Injury     Quarter    

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