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
117458803 11745880 3 F 20160915 20151117 20160926 EXP PHEH2015US023698 NOVARTIS 0.00 F Y 0.00000 20160926 CN 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
117458803 11745880 1 PS ZOFRAN ONDANSETRON HYDROCHLORIDE 1 Transplacental UNK D 20007
117458803 11745880 2 SS ONDANSETRON ONDANSETRON 1 Transplacental UNK D 0 TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
117458803 11745880 1 Foetal exposure during pregnancy
117458803 11745880 2 Foetal exposure during pregnancy

Outcome of event

Event ID CASEID OUTC COD
117458803 11745880 OT
117458803 11745880 CA

Reactions reported

Event ID CASEID DRUG REC ACT PT
117458803 11745880 Anhedonia
117458803 11745880 Anxiety
117458803 11745880 Cleft palate
117458803 11745880 Congenital anomaly
117458803 11745880 Emotional distress
117458803 11745880 Foetal exposure during pregnancy
117458803 11745880 Injury
117458803 11745880 Pain
117458803 11745880 Speech disorder developmental

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found