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
127140671 12714067 1 I 20160525 20160707 20160905 20160905 EXP FR-009507513-1607FRA004271 MERCK 71.74 YR M Y 90.00000 KG 20160905 CN 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
127140671 12714067 1 PS JANUVIA SITAGLIPTIN PHOSPHATE 1 Oral 100 MG, QD Y 21995 100 MG FILM-COATED TABLET QD
127140671 12714067 2 C SOTALOL. SOTALOL 1 80 MG, QD 0 80 MG QD
127140671 12714067 3 C SOTALOL. SOTALOL 1 0
127140671 12714067 4 C LEVOTHYROX LEVOTHYROXINE 1 50 MICROGRAM, QD 0 50 UG QD
127140671 12714067 5 C ESOMEPRAZOLE ESOMEPRAZOLE 1 20 MG, QD 0 20 MG QD
127140671 12714067 6 C EFFERALGAN ACETAMINOPHEN 1 3 G, QD 0 3 G QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127140671 12714067 2 Hypertension
127140671 12714067 3 Tachycardia
127140671 12714067 4 Hypothyroidism
127140671 12714067 5 Gastrooesophageal reflux disease
127140671 12714067 6 Osteoarthritis

Outcome of event

Event ID CASEID OUTC COD
127140671 12714067 HO
127140671 12714067 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127140671 12714067 Hepatic cirrhosis
127140671 12714067 Pancreatitis acute

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
127140671 12714067 1 2011 20160605 0
127140671 12714067 2 2008 0
127140671 12714067 4 2013 0
127140671 12714067 5 2013 0
127140671 12714067 6 2009 0