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
127674061 12767406 1 I 20160908 20160909 20160921 20160921 PER US-BAYER-2016-176940 BAYER 79.00 YR E F Y 61.00000 KG 20160921 OT 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
127674061 12767406 1 PS CLARITIN LORATADINE 1 1 DF, QD CVMB6KX 19658 1 DF TABLET QD
127674061 12767406 2 C AMITIZA LUBIPROSTONE 1 UNK 0
127674061 12767406 3 C METAMUCIL PLANTAGO SEED 1 UNK 0
127674061 12767406 4 C COLACE DOCUSATE SODIUM 1 UNK 0
127674061 12767406 5 C OSTEO BI-FLEX CHONDROITIN SULFATE AGLUCOSAMINE 1 UNK 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127674061 12767406 1 Multiple allergies

Outcome of event

no results found

Reactions reported

Event ID CASEID DRUG REC ACT PT
127674061 12767406 Abdominal pain upper
127674061 12767406 Abnormal faeces
127674061 12767406 Diarrhoea
127674061 12767406 Extra dose administered
127674061 12767406 Frequent bowel movements
127674061 12767406 Middle insomnia

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

no results found

Therapies reported

no results found