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
126813153 12681315 3 F 201608 20160908 20160824 20160916 EXP FR-PFIZER INC-2016389792 PFIZER 70.00 YR M Y 0.00000 20160916 OT FR FR

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
126813153 12681315 1 PS TAHOR ATORVASTATIN CALCIUM 1 Oral 40 MG, DAILY Y 20702 40 MG
126813153 12681315 2 I FUCIDINE FUSIDIC ACID 1 Oral 750 MG, UNK Y 0 750 MG
126813153 12681315 3 I COLCHICINE OPOCALCIUM COLCHICINE 1 1 MG, UNK Y 0 1 MG TABLET
126813153 12681315 4 C DALACINE - PER 2 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126813153 12681315 1 Dyslipidaemia
126813153 12681315 3 Behcet's syndrome

Outcome of event

Event ID CASEID OUTC COD
126813153 12681315 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126813153 12681315 Amyotrophy
126813153 12681315 Contraindicated product administered
126813153 12681315 Diarrhoea
126813153 12681315 Drug interaction
126813153 12681315 Glomerular filtration rate decreased
126813153 12681315 Myalgia
126813153 12681315 Rhabdomyolysis
126813153 12681315 Toxicity to various agents
126813153 12681315 Transaminases increased

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
126813153 12681315 1 20160802 0
126813153 12681315 2 20160720 20160802 0
126813153 12681315 3 20160805 0
126813153 12681315 4 20160720 0