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
126675651 12667565 1 I 201608 20160811 20160819 20160819 EXP US-009507513-1608USA007699 MERCK 63.00 YR M Y 0.00000 20160819 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
126675651 12667565 1 PS BELSOMRA SUVOREXANT 1 Oral 20 MG, AT BEDTIME U 204569 20 MG TABLET QD
126675651 12667565 2 SS OXYCODONE OXYCODONE 1 30 MG, HS U 0 30 MG QD
126675651 12667565 3 SS SOTALOL. SOTALOL 1 80 MG, HS U 0 80 MG QD
126675651 12667565 4 SS PRADAXA DABIGATRAN ETEXILATE MESYLATE 1 150 MG, HS U 0 150 MG QD
126675651 12667565 5 SS LIPITOR ATORVASTATIN CALCIUM 1 20 MG, HS U 0 20 MG QD
126675651 12667565 6 SS RISPERIDONE. RISPERIDONE 1 20 MG, HS U 0 20 MG QD
126675651 12667565 7 SS KLONOPIN CLONAZEPAM 1 1 MG, HS U 0 1 MG QD
126675651 12667565 8 SS TRILEPTAL OXCARBAZEPINE 1 300 MG, HS U 0 300 MG QD

Indications of drugs used

no results found

Outcome of event

Event ID CASEID OUTC COD
126675651 12667565 HO
126675651 12667565 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126675651 12667565 Atrial fibrillation
126675651 12667565 Drug abuse
126675651 12667565 Eye movement disorder
126675651 12667565 Haemoptysis
126675651 12667565 Heart rate decreased
126675651 12667565 Hyperhidrosis
126675651 12667565 Lung disorder
126675651 12667565 Miosis
126675651 12667565 Rhabdomyolysis
126675651 12667565 Somnolence

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

no results found

Therapies reported

no results found