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
117056985 11705698 5 F 20160816 20151106 20160818 PER PHEH2015US022715 NOVARTIS 0.00 F Y 77.98000 KG 20160818 MD 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
117056985 11705698 1 PS ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Oral 4 MG TO 8 MG, THRICE DAILY 20007 8 MG TABLET TID
117056985 11705698 2 SS ONDANSETRON HYDROCHLORIDE. ONDANSETRON HYDROCHLORIDE 1 Oral U 20007 DISPERSIBLE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117056985 11705698 1 Vomiting in pregnancy
117056985 11705698 2 Vomiting in pregnancy

Outcome of event

Event ID CASEID OUTC COD
117056985 11705698 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117056985 11705698 Anxiety
117056985 11705698 Emotional distress
117056985 11705698 Injury
117056985 11705698 Maternal exposure during pregnancy
117056985 11705698 Pain
117056985 11705698 Product use issue

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
117056985 11705698 1 20121106 20131008 0