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
72763255 7276325 5 F 200812 20160706 20100211 20160718 PER US-BAYER-201013570NA BAYER 43.00 YR A F Y 48.00000 KG 20160718 CN 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
72763255 7276325 1 PS YASMIN DROSPIRENONEETHINYL ESTRADIOL 1 Oral UNK UNK, QD Y 81332A 21098 FILM-COATED TABLET QD
72763255 7276325 2 SS YAZ DROSPIRENONEETHINYL ESTRADIOL 1 UNK Y 0 FILM-COATED TABLET
72763255 7276325 3 C PHENTERMINE. PHENTERMINE 1 0
72763255 7276325 4 C DITROPAN OXYBUTYNIN CHLORIDE 1 0
72763255 7276325 5 C B AND O 2 0 SUPPOSITORY
72763255 7276325 6 C VALIUM DIAZEPAM 1 0
72763255 7276325 7 C MECLIZINE MECLIZINE HYDROCHLORIDE 1 0
72763255 7276325 8 C AMMONIUM LACTATE. AMMONIUM LACTATE 1 12 %, UNK 0 12 PCT

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
72763255 7276325 1 Contraception
72763255 7276325 3 Decreased appetite
72763255 7276325 4 Urinary tract infection
72763255 7276325 5 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
72763255 7276325 OT
72763255 7276325 DS
72763255 7276325 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
72763255 7276325 Cerebrovascular accident
72763255 7276325 Cholelithiasis
72763255 7276325 Deep vein thrombosis
72763255 7276325 Ischaemic stroke
72763255 7276325 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
72763255 7276325 1 200708 20081224 0
72763255 7276325 2 200808 200901 0