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
127410901 12741090 1 I 20151008 20160907 20160914 20160914 EXP GB-MHRA-EYC 00144719 GB-MICRO LABS LIMITED-BB2016-01336 MICRO LABS 69.00 YR F Y 69.85000 KG 20160914 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
127410901 12741090 1 PS SIMVASTATIN. SIMVASTATIN 1 Oral Y U 90383 10 MG
127410901 12741090 2 SS NITROFURANTOIN. NITROFURANTOIN 1 Oral DON'T KNOW. NORMAL DOSE FOR CYSTITIS I THINK. U U 0
127410901 12741090 3 C AMITRIPTYLINE AMITRIPTYLINE 1 Unknown 0
127410901 12741090 4 C BECLOMETASONE DIPROPIONATE BECLOMETHASONE DIPROPIONATE 1 Unknown 0
127410901 12741090 5 C CETIRIZINE CETIRIZINE HYDROCHLORIDE 1 Unknown 0
127410901 12741090 6 C COLPERMIN 2 Unknown 0
127410901 12741090 7 C CELECOXIB. CELECOXIB 1 Unknown 0
127410901 12741090 8 C GAVISCON ADVANCE POTASSIUM BICARBONATESODIUM ALGINATE 1 Unknown 0
127410901 12741090 9 C RABEPRAZOLE SODIUM. RABEPRAZOLE SODIUM 1 Unknown 0
127410901 12741090 10 C TEMAZEPAM. TEMAZEPAM 1 Unknown 0
127410901 12741090 11 C TRAMADOL. TRAMADOL 1 Unknown 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127410901 12741090 1 Blood cholesterol increased
127410901 12741090 2 Cystitis
127410901 12741090 3 Product used for unknown indication
127410901 12741090 4 Product used for unknown indication
127410901 12741090 5 Product used for unknown indication
127410901 12741090 6 Product used for unknown indication
127410901 12741090 7 Product used for unknown indication
127410901 12741090 8 Product used for unknown indication
127410901 12741090 9 Product used for unknown indication
127410901 12741090 10 Product used for unknown indication
127410901 12741090 11 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127410901 12741090 OT
127410901 12741090 DS
127410901 12741090 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127410901 12741090 Abdominal distension
127410901 12741090 Abdominal pain
127410901 12741090 Decreased appetite
127410901 12741090 Drug-induced liver injury
127410901 12741090 Malaise

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
127410901 12741090 1 20160412 20160416 0
127410901 12741090 2 20151004 0