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
126039931 12603993 1 I 20160708 20160720 20160728 20160728 EXP GB-MHRA-EYC 00142443 GB-PERRIGO-16GB018336 PERRIGO 0.00 Y 0.00000 20160728 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
126039931 12603993 1 PS LORATADINE. LORATADINE 1 Unknown UNK U U UNKNOWN 76301 TABLET
126039931 12603993 2 SS CHLORHEXIDINE GLUCONATE. CHLORHEXIDINE GLUCONATE 1 Oral 10 ML, BID 20 ML Y U 1066LE0106 0 10 ML
126039931 12603993 3 SS CYCLIZINE CYCLIZINE 1 Intramuscular UNK U U UNKNOWN 0
126039931 12603993 4 SS DIHYDROCODEINE DIHYDROCODEINE 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 5 SS ORAMORPH MORPHINE SULFATE 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 6 SS PREDNISOLONE. PREDNISOLONE 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 7 SS SALBUTAMOL ALBUTEROL 1 Respiratory (inhalation) UNK U U UNKNOWN 0
126039931 12603993 8 SS SERETIDE FLUTICASONE PROPIONATESALMETEROL XINAFOATE 1 Respiratory (inhalation) UNK U U UNKNOWN 0
126039931 12603993 9 SS LYRICA PREGABALIN 1 Unknown 150MG AND 300MG U U UNKNOWN 0
126039931 12603993 10 C ADCAL-D3 CALCIUM CARBONATECHOLECALCIFEROL 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 11 C ALENDRONIC ACID ALENDRONIC ACID 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 12 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 13 C COSMOCOL 2 Unknown UNK U U UNKNWON 0
126039931 12603993 14 C LACTULOSE. LACTULOSE 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 15 C MONTELUKAST MONTELUKAST SODIUM 1 Unknown UNK U U UNKNOWN 0
126039931 12603993 16 C PHENOXYMETHYLPENICILLIN PENICILLIN V 1 Unknown UNK U U UNKNOWN 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126039931 12603993 1 Product used for unknown indication
126039931 12603993 2 Mouth ulceration
126039931 12603993 3 Product used for unknown indication
126039931 12603993 4 Product used for unknown indication
126039931 12603993 5 Product used for unknown indication
126039931 12603993 6 Product used for unknown indication
126039931 12603993 7 Product used for unknown indication
126039931 12603993 8 Product used for unknown indication
126039931 12603993 9 Product used for unknown indication
126039931 12603993 10 Product used for unknown indication
126039931 12603993 11 Product used for unknown indication
126039931 12603993 12 Product used for unknown indication
126039931 12603993 13 Product used for unknown indication
126039931 12603993 14 Product used for unknown indication
126039931 12603993 15 Product used for unknown indication
126039931 12603993 16 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
126039931 12603993 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126039931 12603993 Asthma
126039931 12603993 Drug interaction
126039931 12603993 Feeling abnormal
126039931 12603993 Feeling drunk
126039931 12603993 Oral discomfort
126039931 12603993 Oxygen saturation decreased
126039931 12603993 Swelling face

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
126039931 12603993 2 20160708 20160708 0