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
127571881 12757188 1 I 20160905 20160914 20160919 20160919 EXP MX-ROCHE-1831036 ROCHE 47.00 YR F Y 53.50000 KG 20160919 CN MX MX

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
127571881 12757188 1 PS RIVOTRIL CLONAZEPAM 1 Oral 7:00AM(5 DROPS),1:00PM(5 DROPS),9:00PM(9 DROPS) 17533 TID
127571881 12757188 2 C VITAMIN E .ALPHA.-TOCOPHEROL 1 Oral 0 CAPSULE QD
127571881 12757188 3 C OMEGA 3 OMEGA-3 FATTY ACIDS 1 Oral 0 CAPSULE QD
127571881 12757188 4 C YASMIN DROSPIRENONEETHINYL ESTRADIOL 1 Oral DURING 21 DAYS OF TREATMENT AND 7 DAYS OF REST 0 QD
127571881 12757188 5 C PRISTIQ EXTENDED-RELEASE DESVENLAFAXINE SUCCINATE 1 Oral 7:00AM (1 TABLET) 0 50 MG TABLET QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127571881 12757188 1 Anxiety
127571881 12757188 2 Nutritional supplementation
127571881 12757188 3 Nutritional supplementation
127571881 12757188 5 Anxiety

Outcome of event

Event ID CASEID OUTC COD
127571881 12757188 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127571881 12757188 Angina pectoris
127571881 12757188 Hallucination
127571881 12757188 Insomnia
127571881 12757188 Oropharyngeal pain

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
127571881 12757188 1 20160905 0
127571881 12757188 2 2012 0
127571881 12757188 3 2012 0
127571881 12757188 4 201606 0
127571881 12757188 5 20160905 0