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
126809612 12680961 2 F 20160905 20160824 20160919 EXP GB-TEVA-686896ISR TEVA GOLDIE FC, BROGAN A, BOYLE JG. CIPROFLOXACIN AND STATIN INTERACTION: A CAUTIONARY TALE OF RHABDOMYOLYSIS. BMJ CASE REPORTS. 2016; ARTICLE NUMBER BCR2016216048 62.00 YR F Y 0.00000 20160919 MD GB GB

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
126809612 12680961 1 PS SIMVASTATIN. SIMVASTATIN 1 40 MG NOCTE Y 76052 40 MG
126809612 12680961 2 I CIPROFLOXACIN. CIPROFLOXACIN 1 U 74124
126809612 12680961 3 C Nicorandil NICORANDIL 1 20 MILLIGRAM DAILY; 0 10 MG BID
126809612 12680961 4 C ASPIRIN. ASPIRIN 1 75 MILLIGRAM DAILY; 0 75 MG QD
126809612 12680961 5 C Bisoprolol BISOPROLOL 1 5 MILLIGRAM DAILY; 0 5 MG QD
126809612 12680961 6 C NITROGLYCERIN. NITROGLYCERIN 1 AS NEEDED 0 400 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126809612 12680961 2 Urinary tract infection

Outcome of event

Event ID CASEID OUTC COD
126809612 12680961 OT
126809612 12680961 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126809612 12680961 Blood creatine phosphokinase increased
126809612 12680961 Drug interaction
126809612 12680961 Hepatic function abnormal
126809612 12680961 Muscular weakness
126809612 12680961 Rhabdomyolysis

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

no results found

Therapies reported

no results found