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
126890771 12689077 1 I 20160720 20160729 20160826 20160826 PER US-TEVA-682034ACC TEVA 50.17 YR F Y 64.92000 KG 20160826 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
126890771 12689077 1 PS PLAN B ONE-STEP LEVONORGESTREL 1 Y 21998 1.5 MG TABLET
126890771 12689077 2 C TAGAMET CIMETIDINE 1 0
126890771 12689077 3 C TOPAMAX TOPIRAMATE 1 0
126890771 12689077 4 C VITAMIN B COMPLEX CYANOCOBALAMINDEXPANTHENOLNIACINAMIDEPYRIDOXINE HYDROCHLORIDERIBOFLAVIN 5'-PHOSPHATE SODIUMTHIAMINE HYDROCHLORIDEVITAMIN B COMPLEX 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126890771 12689077 1 Post coital contraception
126890771 12689077 2 Gastric pH
126890771 12689077 3 Antioxidant therapy

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126890771 12689077 Back pain
126890771 12689077 Diarrhoea
126890771 12689077 Dizziness
126890771 12689077 Dysmenorrhoea
126890771 12689077 Menstruation irregular
126890771 12689077 Vaginal haemorrhage

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

no results found

Therapies reported

no results found