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
127328701 12732870 1 I 20160809 0 20160911 20160911 DIR US-FDA-350316 FDA-CTU 18.00 YR F N 53.55000 KG 20160911 N 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
127328701 12732870 1 PS NAPROXEN. NAPROXEN 1 Oral 20 TABLET TWICE A DAY ORAL N D 20170713 0 20 DF COATED TABLET BID
127328701 12732870 3 C BIRTH CONTROL UNSPECIFIED INGREDIENT 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127328701 12732870 1 Dysmenorrhoea

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127328701 12732870 Cognitive disorder
127328701 12732870 Confusional state
127328701 12732870 Dizziness
127328701 12732870 Feeling abnormal
127328701 12732870 Hypoacusis
127328701 12732870 Lymphadenopathy
127328701 12732870 Migraine
127328701 12732870 Neck pain
127328701 12732870 Presyncope
127328701 12732870 Vision blurred
127328701 12732870 Visual impairment

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
127328701 12732870 1 20160809 20160809 0