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
126062541 12606254 1 I 20160711 20160720 20160729 20160729 EXP GB-ACTAVIS-2016-16419 WATSON 77.00 YR F Y 0.00000 20160729 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
126062541 12606254 1 SS Atorvastatin (Unknown) ATORVASTATIN 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 2 SS Betahistine (Unknown) BETAHISTINE 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 3 SS Bisoprolol (Unknown) BISOPROLOL 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 4 SS Levothyroxine (Unknown) LEVOTHYROXINE 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 5 SS MONTELUKAST MONTELUKAST SODIUM 1 Unknown UNK U UNCONFIRMED 0
126062541 12606254 6 PS Omeprazole (Unknown) OMEPRAZOLE 1 Oral UNK U UNCONFIRMED 75347 UNK
126062541 12606254 7 SS Prednisolone (Unknown) PREDNISOLONE 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 8 SS Pregabalin (Unknown) PREGABALIN 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 9 SS Thiamine (Unknown) THIAMINE 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 10 SS Zopiclone (Unknown) ZOPICLONE 1 Unknown UNK U UNCONFIRMED 0 UNK
126062541 12606254 11 SS ELIQUIS APIXABAN 1 Unknown UNK U 0
126062541 12606254 12 SS FERROUS GLUCONATE FERROUS GLUCONATE 1 Unknown UNK U 0
126062541 12606254 13 SS LINAGLIPTIN LINAGLIPTIN 1 Unknown UNK U 0
126062541 12606254 14 SS UMECLIDINIUM UMECLIDINIUM BROMIDE 1 Unknown UNK U 0
126062541 12606254 15 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Unknown UNK U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126062541 12606254 1 Product used for unknown indication
126062541 12606254 2 Product used for unknown indication
126062541 12606254 3 Product used for unknown indication
126062541 12606254 4 Product used for unknown indication
126062541 12606254 5 Product used for unknown indication
126062541 12606254 6 Product used for unknown indication
126062541 12606254 7 Product used for unknown indication
126062541 12606254 8 Product used for unknown indication
126062541 12606254 9 Product used for unknown indication
126062541 12606254 10 Product used for unknown indication
126062541 12606254 11 Product used for unknown indication
126062541 12606254 12 Product used for unknown indication
126062541 12606254 13 Product used for unknown indication
126062541 12606254 14 Product used for unknown indication
126062541 12606254 15 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126062541 12606254 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
126062541 12606254 Cough
126062541 12606254 Lethargy
126062541 12606254 Sputum discoloured

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

no results found

Therapies reported

no results found