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
126997021 12699702 1 I 2012 20160816 20160830 20160830 EXP US-DEPOMED, INC.-US-2016DEP011772 DEPOMED 0.00 Y 0.00000 20160830 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
126997021 12699702 1 PS GRALISE GABAPENTIN 1 Oral 300 MG, QD, TITRATED UP TO 1200 MG 22544 300 MG TABLET
126997021 12699702 2 SS GRALISE GABAPENTIN 1 Oral 300 MG, UNK, TITRATED UP TO 1200 MG 22544 300 MG TABLET
126997021 12699702 3 SS GRALISE GABAPENTIN 1 Oral 300 MG, QD, TITRATED UP TO 1200 MG 22544 300 MG TABLET
126997021 12699702 4 SS GRALISE GABAPENTIN 1 Oral 300 MG, QD, TITRATED UP TO 1200 MG 22544 300 MG TABLET
126997021 12699702 5 SS GABAPENTIN. GABAPENTIN 1 600 MG, TID 0 600 MG
126997021 12699702 6 SS GABAPENTIN. GABAPENTIN 1 600 MG, TID 0 600 MG
126997021 12699702 7 SS GABAPENTIN. GABAPENTIN 1 600 MG, TID 0 600 MG
126997021 12699702 8 C ELIQUIS APIXABAN 1 Oral 2.5 MG, BID 0 2.5 MG TABLET
126997021 12699702 9 C SOTALOL. SOTALOL 1 Oral 80 MG, QD 0 80 MG TABLET
126997021 12699702 10 C SOTALOL. SOTALOL 1 Oral 40 MG, QD 0 40 MG TABLET
126997021 12699702 11 C LOSARTAN POTASSSIUM 2 Oral 50 MG, QD 0 50 MG TABLET
126997021 12699702 12 C ASPIRIN. ASPIRIN 1 Oral 81 MG, QD 0 81 MG TABLET
126997021 12699702 13 C TRAMADOL. TRAMADOL 1 Oral 50 MG, TID, PRN 0 50 MG TABLET

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126997021 12699702 1 Neck pain
126997021 12699702 5 Product used for unknown indication
126997021 12699702 8 Atrial fibrillation
126997021 12699702 9 Atrial fibrillation
126997021 12699702 11 Hypertension
126997021 12699702 12 Atrial fibrillation
126997021 12699702 13 Back pain

Outcome of event

Event ID CASEID OUTC COD
126997021 12699702 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126997021 12699702 Adverse event
126997021 12699702 Barrett's oesophagus
126997021 12699702 Bone neoplasm
126997021 12699702 Dizziness
126997021 12699702 Drug dose titration not performed
126997021 12699702 Drug ineffective for unapproved indication
126997021 12699702 Dysphagia
126997021 12699702 Dyspnoea
126997021 12699702 Gastrooesophageal reflux disease
126997021 12699702 Grief reaction
126997021 12699702 Headache
126997021 12699702 Hypertension
126997021 12699702 Malignant melanoma
126997021 12699702 Nausea
126997021 12699702 Neuralgia
126997021 12699702 Oedema
126997021 12699702 Product use issue
126997021 12699702 Throat cancer
126997021 12699702 Tonsillar neoplasm

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
126997021 12699702 1 2012 0
126997021 12699702 4 201505 0
126997021 12699702 8 2012 0
126997021 12699702 9 2012 0
126997021 12699702 10 2012 0
126997021 12699702 11 2011 0
126997021 12699702 12 2010 0