The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8553833 8694665 I 8553833-4 20120624 20120727 20120731 PER US-TEVA-351071USA TEVA YR F Y 20120731 CN UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8553833 1020402952 SS PLAN B ONE-STEP 1 ORAL 1.5 MILLIGRAM; 021998
8553833 1020402953 C MULTI-VITAMIN 1
8553833 1020402951 SS PLAN B ONE-STEP 1 ORAL 1.5 MILLIGRAM; 021998
8553833 1020402949 PS PLAN B ONE-STEP 1 ORAL 1.5 MILLIGRAM; 021998
8553833 1020402950 SS PLAN B ONE-STEP 1 ORAL 1.5 MILLIGRAM; 021998

Indications of drugs used

Event ID DRUG SEQ INDI PT
8553833 1020402953 MEDICAL DIET
8553833 1020402949 POST COITAL CONTRACEPTION

Outcome of event

no results found

Reactions reported

Event ID PT
8553833 BREAST CYST
8553833 MENSTRUATION IRREGULAR
8553833 MENSTRUATION DELAYED
8553833 FIBROADENOMA OF BREAST

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8553833 1020402952 20120722 20120722
8553833 1020402951 20120714 20120714
8553833 1020402949 20120612 20120612
8553833 1020402950 20120617 20120617