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
100372613 10037261 3 F 20060926 20141222 20140326 20141231 PER US-BAYER-2014-044970 BAYER 36.00 YR A F Y 55.00000 KG 20141231 N OT 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
100372613 10037261 1 PS YASMIN DROSPIRENONEETHINYL ESTRADIOL 1 ORAL UNK D 21098 FILM-COATED TABLET
100372613 10037261 2 C LEXAPRO ESCITALOPRAM OXALATE 1 ORAL UNK D 0
100372613 10037261 3 C PEPCID FAMOTIDINE 1 D 0
100372613 10037261 4 C DOCUSATE DOCUSATE 1 D 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
100372613 10037261 1 Contraception
100372613 10037261 2 Antidepressant therapy

Outcome of event

Event ID CASEID OUTC COD
100372613 10037261 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
100372613 10037261 Aphagia
100372613 10037261 Balance disorder
100372613 10037261 Bradyphrenia
100372613 10037261 Cerebrovascular accident
100372613 10037261 Diplopia
100372613 10037261 Dysphonia
100372613 10037261 Fatigue
100372613 10037261 Gait disturbance
100372613 10037261 Hemiplegia
100372613 10037261 Hypoaesthesia
100372613 10037261 Injury
100372613 10037261 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
100372613 10037261 1 200403 200609 0
100372613 10037261 2 200508 200908 0