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
117176497 11717649 7 F 20160922 20151110 20160929 EXP PHEH2015US022852 NOVARTIS 0.00 F Y 0.00000 20160929 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
117176497 11717649 1 PS ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Oral 8 MG, UNK 20007 8 MG
117176497 11717649 2 SS ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Unknown UNK 20007
117176497 11717649 3 SS ONDANSETRON HYDROCHLORIDE. ONDANSETRON HYDROCHLORIDE 1 Oral 8 MG, UNK 0 8 MG DISPERSIBLE TABLET
117176497 11717649 4 SS ONDANSETRON ONDANSETRON 1 Oral U 0 DISPERSIBLE TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117176497 11717649 1 Vomiting in pregnancy
117176497 11717649 3 Product used for unknown indication
117176497 11717649 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
117176497 11717649 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
117176497 11717649 Anxiety
117176497 11717649 Cystitis
117176497 11717649 Emotional distress
117176497 11717649 Injury
117176497 11717649 Maternal exposure during pregnancy
117176497 11717649 Pain
117176497 11717649 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
117176497 11717649 1 20140520 20140621 0
117176497 11717649 2 201410 0
117176497 11717649 3 20140520 20140621 0