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
126192741 12619274 1 I 201607 20160728 20160803 20160803 EXP SE-MPA-2016-004362 SE-BAYER-2016-147026 BAYER 27.00 YR A F Y 0.00000 20160803 CN SE SE

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
126192741 12619274 1 PS YAZ DROSPIRENONEETHINYL ESTRADIOL 1 N 21676 FILM-COATED TABLET
126192741 12619274 2 SS YAZ DROSPIRENONEETHINYL ESTRADIOL 1 N 21676 FILM-COATED TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126192741 12619274 1 Menstruation irregular
126192741 12619274 2 Mood swings

Outcome of event

Event ID CASEID OUTC COD
126192741 12619274 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126192741 12619274 Acne
126192741 12619274 Anorgasmia
126192741 12619274 Asthenia
126192741 12619274 Breast enlargement
126192741 12619274 Decreased appetite
126192741 12619274 Diarrhoea
126192741 12619274 Dizziness
126192741 12619274 Flatulence
126192741 12619274 Formication
126192741 12619274 Hot flush
126192741 12619274 Hyperhidrosis
126192741 12619274 Libido decreased
126192741 12619274 Mood swings
126192741 12619274 Nausea
126192741 12619274 Nervousness
126192741 12619274 Palpitations
126192741 12619274 Panic attack
126192741 12619274 Tremor
126192741 12619274 Vaginal haemorrhage

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
126192741 12619274 1 20160710 0