The Safety Rates Drug Report

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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
125907194 12590719 4 F 20160711 20160819 20160726 20160825 EXP GB-BRISTOL-MYERS SQUIBBCOMPANY-BMS-2016-058787 GB-GLENMARK PHARMACEUTICALS INC, USA.-2016GMK023712 GLENMARK 0.00 Y 0.00000 20160825 OT GB GB

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
125907194 12590719 1 PS MONTELUKAST SODIUM. MONTELUKAST SODIUM 1 Unknown UNK U 90926
125907194 12590719 2 SS OMEPRAZOLE. OMEPRAZOLE 1 Oral UNK U 0
125907194 12590719 3 SS ATORVASTATIN CALCIUM. ATORVASTATIN CALCIUM 1 Unknown UNK U 0
125907194 12590719 4 SS BETAHISTINE BETAHISTINE 1 Unknown UNK U 0
125907194 12590719 5 SS BISOPROLOL FUMARATE. BISOPROLOL FUMARATE 1 Unknown UNK U 0
125907194 12590719 6 SS ELIQUIS APIXABAN 1 Unknown UNK U 0
125907194 12590719 7 SS FERROUS GLUCONATE FERROUS GLUCONATE 1 Unknown UNK U 0
125907194 12590719 8 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown UNK U 0
125907194 12590719 9 SS LINAGLIPTIN LINAGLIPTIN 1 Unknown UNK U 0
125907194 12590719 10 SS PREDNISOLONE. PREDNISOLONE 1 Unknown UNK U 0
125907194 12590719 11 SS PREGABALIN. PREGABALIN 1 Unknown UNK U 0
125907194 12590719 12 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK U 0
125907194 12590719 13 SS THIAMINE. THIAMINE 1 Unknown UNK U 0
125907194 12590719 14 SS UMECLIDINIUM UMECLIDINIUM BROMIDE 1 Unknown UNK U 0
125907194 12590719 15 SS ZOPICLONE ZOPICLONE 1 Unknown UNK U 0
125907194 12590719 16 SS ATORVASTATIN ATORVASTATIN 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
125907194 12590719 1 Product used for unknown indication
125907194 12590719 2 Product used for unknown indication
125907194 12590719 3 Product used for unknown indication
125907194 12590719 4 Product used for unknown indication
125907194 12590719 5 Product used for unknown indication
125907194 12590719 6 Product used for unknown indication
125907194 12590719 7 Product used for unknown indication
125907194 12590719 8 Product used for unknown indication
125907194 12590719 9 Product used for unknown indication
125907194 12590719 10 Product used for unknown indication
125907194 12590719 11 Product used for unknown indication
125907194 12590719 12 Product used for unknown indication
125907194 12590719 13 Product used for unknown indication
125907194 12590719 14 Product used for unknown indication
125907194 12590719 15 Product used for unknown indication
125907194 12590719 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
125907194 12590719 HO
125907194 12590719 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
125907194 12590719 Cough
125907194 12590719 Lethargy
125907194 12590719 Sputum discoloured

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

no results found

Therapies reported

no results found