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
126102213 12610221 3 F 20160711 20160819 20160801 20160823 EXP GB-MYLANLABS-2016M1030209 MYLAN 0.00 Y 0.00000 20160823 CN 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
126102213 12610221 1 PS ATORVASTATIN ATORVASTATIN 1 Unknown UNK U U 91226
126102213 12610221 2 SS BETAHISTINE BETAHISTINE 1 Unknown UNK U U 0
126102213 12610221 3 SS BISOPROLOL BISOPROLOL 1 Unknown UNK U U 0
126102213 12610221 4 SS MONTELUKAST MONTELUKAST SODIUM 1 Unknown UNK U U 0
126102213 12610221 5 SS PREDNISOLONE. PREDNISOLONE 1 Unknown UNK U U 0
126102213 12610221 6 SS PREGABALIN. PREGABALIN 1 Unknown UNK U U 0
126102213 12610221 7 SS FLUTICASONE FLUTICASONEFLUTICASONE PROPIONATE 1 Unknown UNK U U 0
126102213 12610221 8 SS THIAMINE MYLAN THIAMINE 1 Unknown UNK U U 0
126102213 12610221 9 SS ZOPICLONE ZOPICLONE 1 Unknown UNK U U 0
126102213 12610221 10 SS OMEPRAZOLE. OMEPRAZOLE 1 Unknown UNK U U 0
126102213 12610221 11 SS ELIQUIS APIXABAN 1 Unknown UNK U U 0
126102213 12610221 12 SS FERROUS GLUCONATE FERROUS GLUCONATE 1 Unknown UNK U U 0
126102213 12610221 13 SS LEVOTHYROXINE. LEVOTHYROXINE 1 Unknown UNK U U 0
126102213 12610221 14 SS LINAGLIPTIN LINAGLIPTIN 1 Unknown UNK U U 0
126102213 12610221 15 C UMECLIDINIUM UMECLIDINIUM BROMIDE 1 Unknown UNK U U 0
126102213 12610221 16 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK U U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126102213 12610221 1 Product used for unknown indication
126102213 12610221 2 Product used for unknown indication
126102213 12610221 3 Product used for unknown indication
126102213 12610221 4 Product used for unknown indication
126102213 12610221 6 Product used for unknown indication
126102213 12610221 9 Product used for unknown indication
126102213 12610221 10 Product used for unknown indication
126102213 12610221 11 Product used for unknown indication
126102213 12610221 12 Product used for unknown indication
126102213 12610221 13 Product used for unknown indication
126102213 12610221 14 Product used for unknown indication
126102213 12610221 15 Product used for unknown indication
126102213 12610221 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126102213 12610221 HO
126102213 12610221 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126102213 12610221 Cough
126102213 12610221 Lethargy
126102213 12610221 Sputum discoloured

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

no results found

Therapies reported

no results found