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
111772172 11177217 2 F 20160822 20150610 20160829 EXP RU-BAYER-2015-053991 BAYER 32.00 YR A F Y 0.00000 20160829 CN RU RU

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
111772172 11177217 1 PS YAZ DROSPIRENONEETHINYL ESTRADIOL 1 Oral UNK 21676 FILM-COATED TABLET
111772172 11177217 2 SS Yaz Plus DROSPIRENONEETHINYL ESTRADIOL 1 Oral UNK 0 FILM-COATED TABLET

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
111772172 11177217 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
111772172 11177217 Abnormal withdrawal bleeding
111772172 11177217 Abortion threatened
111772172 11177217 Adverse event
111772172 11177217 Blood bilirubin increased
111772172 11177217 Drug dose omission
111772172 11177217 Exposure during pregnancy
111772172 11177217 Extra dose administered
111772172 11177217 Hyperaesthesia
111772172 11177217 Libido decreased
111772172 11177217 Menstrual disorder
111772172 11177217 Metrorrhagia
111772172 11177217 Mood swings
111772172 11177217 Placental disorder
111772172 11177217 Pregnancy on oral contraceptive
111772172 11177217 Premature baby
111772172 11177217 Premenstrual syndrome
111772172 11177217 Product use issue
111772172 11177217 Retained placenta or membranes
111772172 11177217 Scar
111772172 11177217 Skin reaction

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

no results found

Therapies reported

no results found