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
125209952 12520995 2 F 201507 20160831 20160701 20160905 EXP JP-009507513-1607JPN000111 MERCK 0.00 E F Y 0.00000 20160905 CN JP JP

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
125209952 12520995 1 PS GLACTIV SITAGLIPTIN 1 Oral UNK N 21995 FILM-COATED TABLET
125209952 12520995 2 SS AMLODIN (amlodipine besylate) AMLODIPINE BESYLATE 1 Oral UNK U 0
125209952 12520995 3 SS DEPAS ETIZOLAM 1 Oral UNK U 0
125209952 12520995 4 C CARBOCYSTEINE CARBOCYSTEINE 1 UNK 0
125209952 12520995 5 C LEVOFLOXACIN. LEVOFLOXACIN 1 UNK 0
125209952 12520995 6 C METHYLPREDNISOLONE. METHYLPREDNISOLONE 1 12 MG, QD 0 12 MG QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125209952 12520995 1 Type 2 diabetes mellitus
125209952 12520995 2 Hypertension
125209952 12520995 3 Hypertension

Outcome of event

Event ID CASEID OUTC COD
125209952 12520995 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
125209952 12520995 Hyperglycaemia
125209952 12520995 Interstitial lung disease

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
125209952 12520995 1 201406 201603 0
125209952 12520995 2 201406 0
125209952 12520995 3 2014 0