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
127874621 12787462 1 I 201509 20160913 20160928 20160928 EXP GB-SUN PHARMACEUTICAL INDUSTRIES LTD-2016RR-124464 RANBAXY 74.00 YR M Y 0.00000 20160928 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
127874621 12787462 1 PS LANSOPRAZOLE. LANSOPRAZOLE 1 Unknown 15 MG, QD 202637 15 MG
127874621 12787462 2 SS LANSOPRAZOLE. LANSOPRAZOLE 1 30 MG, BID 202637 30 MG Q12H
127874621 12787462 3 C PARACETAMOL ACETAMINOPHEN 1 Unknown U U 0 500 MG
127874621 12787462 4 C ATORVASTATIN ATORVASTATIN 1 Unknown U U 0 20 MG
127874621 12787462 5 C HALOPERIDOL. HALOPERIDOL 1 Unknown 0.5 MG, UNK U U 0 .5 MG
127874621 12787462 6 C NAPROXEN. NAPROXEN 1 Unknown LONG TERM U U 0 250 MG Q12H
127874621 12787462 7 C LOPRAZOLAM LOPRAZOLAM 1 Unknown HALF A TABLET AT NIGHT. U U 0 1 MG
127874621 12787462 8 C COLCHICINE. COLCHICINE 1 Unknown U U 0 500 UG
127874621 12787462 9 C RANITIDINE. RANITIDINE 1 Unknown 150 MG, BID U U 0 150 MG Q12H
127874621 12787462 10 C ALLOPURINOL. ALLOPURINOL 1 Unknown AT NIGHT. U U 0 300 MG
127874621 12787462 11 C QUININE SULPHATE QUININE SULFATE 1 Unknown AT NIGHT. U U 0 200 MG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127874621 12787462 1 Prophylaxis against gastrointestinal ulcer
127874621 12787462 3 Product used for unknown indication
127874621 12787462 4 Product used for unknown indication
127874621 12787462 5 Product used for unknown indication
127874621 12787462 6 Osteoarthritis
127874621 12787462 7 Product used for unknown indication
127874621 12787462 8 Product used for unknown indication
127874621 12787462 9 Product used for unknown indication
127874621 12787462 10 Product used for unknown indication
127874621 12787462 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127874621 12787462 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
127874621 12787462 Abnormal faeces
127874621 12787462 Abnormal loss of weight
127874621 12787462 Change of bowel habit
127874621 12787462 Decreased appetite
127874621 12787462 Diarrhoea
127874621 12787462 Diverticulum
127874621 12787462 Dizziness
127874621 12787462 Dry mouth
127874621 12787462 Fatigue
127874621 12787462 Flatulence
127874621 12787462 Gastritis
127874621 12787462 Haemoglobin decreased
127874621 12787462 Liver function test abnormal
127874621 12787462 Nausea
127874621 12787462 Pruritus
127874621 12787462 Skin haemorrhage
127874621 12787462 Vomiting

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
127874621 12787462 1 201508 201510 0
127874621 12787462 2 201510 201607 0