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
126098501 12609850 1 I 20160729 20160801 20160801 EXP US-SCIEGEN PHARMACEUTICALS INC-2016SCILIT00343 SCIEGEN 60.00 YR F Y 0.00000 20160801 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
126098501 12609850 1 PS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Unknown 40 MG, UNK FOR SEVERAL YEARS Y U 205519 40 MG TABLET
126098501 12609850 2 I JANUVIA SITAGLIPTIN PHOSPHATE 1 Unknown 100 MG, UNK Y U 0 100 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126098501 12609850 1 Hyperlipidaemia
126098501 12609850 2 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126098501 12609850 OT
126098501 12609850 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126098501 12609850 Acute kidney injury
126098501 12609850 Asthenia
126098501 12609850 Chest pain
126098501 12609850 Chills
126098501 12609850 Drug interaction
126098501 12609850 Myalgia
126098501 12609850 Oedema peripheral
126098501 12609850 Pyrexia
126098501 12609850 Rhabdomyolysis
126098501 12609850 Sinus tachycardia
126098501 12609850 Viral infection

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

no results found

Therapies reported

no results found