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
127956941 12795694 1 I 20160923 20160929 20160929 EXP GB-MHRA-EYC 00145577 GB-MYLANLABS-2016M1041324 MYLAN 0.00 Y 0.00000 20160929 CN 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
127956941 12795694 1 PS ATORVASTATIN ATORVASTATIN 1 Oral UNK (LOW) Y U 91226
127956941 12795694 2 C METFORMIN METFORMIN HYDROCHLORIDE 1 UNK U 0
127956941 12795694 3 C INSULIN INSULIN NOS 1 UNK U 0
127956941 12795694 4 C LORATADINE. LORATADINE 1 UNK U 0
127956941 12795694 5 C ANTIHYPERTENSIVES UNSPECIFIED INGREDIENT 1 UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127956941 12795694 1 Blood cholesterol increased
127956941 12795694 2 Diabetes mellitus
127956941 12795694 3 Diabetes mellitus
127956941 12795694 5 Hypertension

Outcome of event

Event ID CASEID OUTC COD
127956941 12795694 DS
127956941 12795694 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127956941 12795694 Arthralgia
127956941 12795694 Back pain
127956941 12795694 Fatigue
127956941 12795694 Hypoaesthesia
127956941 12795694 Myalgia

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
127956941 12795694 1 20100601 20160909 0