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
127868521 12786852 1 I 20160914 20160928 20160928 PER US-009507513-1609USA007285 MERCK 0.00 A Y 0.00000 20160928 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
127868521 12786852 1 PS REMERON MIRTAZAPINE 1 Unknown UNK U 20415 TABLET
127868521 12786852 2 SS TRINTELLIX VORTIOXETINE HYDROBROMIDE 1 Unknown UNK 0 TABLET
127868521 12786852 3 C RESTORIL TEMAZEPAM 1 UNK 0
127868521 12786852 4 C CELEXA CITALOPRAM HYDROBROMIDE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127868521 12786852 1 Product used for unknown indication
127868521 12786852 2 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127868521 12786852 Decreased appetite
127868521 12786852 Depression
127868521 12786852 Feeding disorder
127868521 12786852 Vomiting

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

no results found

Therapies reported

no results found