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
126763801 12676380 1 I 20160720 20160808 20160823 20160823 EXP US-LUPIN PHARMACEUTICALS INC.-2016-03634 LUPIN 71.63 YR F Y 63.50000 KG 20160823 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
126763801 12676380 1 PS Lovastatin Tablets USP 10 mg LOVASTATIN 1 Unknown UNKNOWN 78296 10 MG QD
126763801 12676380 2 C CHANTIX VARENICLINE TARTRATE 1 Oral F10164430 0 1 MG BID
126763801 12676380 3 C CHANTIX VARENICLINE TARTRATE 1 Unknown F10164430 0
126763801 12676380 4 C Atenolol/HCTZ ATENOLOL 1 Oral 50/25 MG 0 QD
126763801 12676380 5 C VITAMIN D3 CHOLECALCIFEROL 1 Unknown 0
126763801 12676380 6 C Iron pill IRON 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126763801 12676380 1 Blood cholesterol increased
126763801 12676380 2 Tobacco user
126763801 12676380 4 Hypertension
126763801 12676380 5 Product used for unknown indication
126763801 12676380 6 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126763801 12676380 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126763801 12676380 Aneurysm
126763801 12676380 Asthenia
126763801 12676380 Blood cholesterol increased
126763801 12676380 Blood triglycerides increased
126763801 12676380 Drug ineffective
126763801 12676380 Intervertebral disc protrusion

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
126763801 12676380 1 201605 0