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
126699001 12669900 1 I 20160713 20160725 20160820 20160820 PER US-TEVA-680848ACC TEVA 39.65 YR F Y 72.64000 KG 20160820 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
126699001 12669900 1 PS PLAN B ONE-STEP LEVONORGESTREL 1 21998 1.5 MG TABLET
126699001 12669900 2 C SINGULAIR MONTELUKAST SODIUM 1 0
126699001 12669900 3 C CLARITIN LORATADINE 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126699001 12669900 1 Post coital contraception
126699001 12669900 2 Asthma
126699001 12669900 3 Hypersensitivity

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
126699001 12669900 Abdominal distension
126699001 12669900 Menstruation delayed
126699001 12669900 Menstruation irregular
126699001 12669900 Muscle spasms
126699001 12669900 Nausea
126699001 12669900 Premenstrual syndrome
126699001 12669900 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
126699001 12669900 1 20160711 20160711 0