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
119827353 11982735 3 F 2010 20160503 20160201 20160718 EXP US-BAYER-2016-015488 BAYER 26.00 YR A F Y 68.00000 KG 20160715 MD 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
119827353 11982735 1 PS YAZ DROSPIRENONEETHINYL ESTRADIOL 1 Oral UNK 21676 FILM-COATED TABLET
119827353 11982735 2 C KEPPRA LEVETIRACETAM 1 UNK 0
119827353 11982735 3 C DORZOLAMIDE DORZOLAMIDE 1 UNK 0
119827353 11982735 4 C LATANOPROST. LATANOPROST 1 UNK 0

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
119827353 11982735 HO
119827353 11982735 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
119827353 11982735 Anxiety
119827353 11982735 Benign intracranial hypertension
119827353 11982735 Blindness
119827353 11982735 Depression
119827353 11982735 Epilepsy
119827353 11982735 Seizure
119827353 11982735 Thrombosis
119827353 11982735 Visual acuity reduced

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
119827353 11982735 1 200601 201008 0
119827353 11982735 2 2012 0
119827353 11982735 3 2012 0
119827353 11982735 4 2012 0