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
120954614 12095461 4 F 201510 20160923 20160219 20160930 EXP FR-SA-2016SA030585 AVENTIS 44.00 YR A F Y 0.00000 20160930 OT FR FR

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
120954614 12095461 1 PS STILNOX ZOLPIDEM TARTRATE 1 Unknown UNKNOWN 19908
120954614 12095461 2 SS VALDOXAN AGOMELATINE 1 Oral UNKNOWN 0
120954614 12095461 3 SS XEROQUEL QUETIAPINE FUMARATE 1 Unknown UNKNOWN 0
120954614 12095461 4 SS VALIUM DIAZEPAM 1 Unknown UNKNOWN 0
120954614 12095461 5 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown UNKNOWN 0 2 DF TABLET
120954614 12095461 6 SS EFFEXOR VENLAFAXINE HYDROCHLORIDE 1 Unknown UNKNOWN 0 1 DF TABLET
120954614 12095461 7 SS ATARAX HYDROXYZINEHYDROXYZINE HYDROCHLORIDE 1 Unknown UNKNOWN 0
120954614 12095461 8 SS LOXAPAC LOXAPINE SUCCINATE 1 Unknown UNKNOWN 0
120954614 12095461 9 SS NOCTAMIDE LORMETAZEPAM 1 Unknown UNKNOWN 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
120954614 12095461 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
120954614 12095461 Cholestasis
120954614 12095461 Gamma-glutamyltransferase increased
120954614 12095461 Nausea

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
120954614 12095461 2 2013 0
120954614 12095461 3 2013 0
120954614 12095461 4 2013 0
120954614 12095461 5 2013 0
120954614 12095461 7 2013 0