The Safety Rates Drug Report

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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
125897121 12589712 1 I 201404 20160509 20160725 20160725 PER US-APOTEX-2016AP008375 APOTEX 0.00 F Y 0.00000 20160725 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
125897121 12589712 1 PS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Unknown 20 MG, QD 90548 20 MG TABLET
125897121 12589712 2 SS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Unknown 10 MG, ONCE DAILY IN THE EVENING 90548 10 MG TABLET QD
125897121 12589712 3 C COMBIGAN BRIMONIDINE TARTRATETIMOLOL MALEATE 1 Unknown AT MORNING AND NIGHT U U 0 BID
125897121 12589712 4 C LUMIGAN BIMATOPROST 1 Unknown UNK, Q.H.S. U U 0 QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125897121 12589712 1 Blood cholesterol increased
125897121 12589712 3 Eye disorder
125897121 12589712 4 Product used for unknown indication

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
125897121 12589712 Condition aggravated
125897121 12589712 Gait disturbance
125897121 12589712 Muscle disorder
125897121 12589712 Product substitution issue

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
125897121 12589712 1 201404 0