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
127356912 12735691 2 F 20160912 20160913 20160915 EXP NO-ALVOGEN-2016-ALVOGEN-028378 ALVOGEN 63.00 YR F Y 0.00000 20160915 PH NO NO

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
127356912 12735691 1 PS ATENOLOL. ATENOLOL 1 Y 18240 50 MG QD
127356912 12735691 2 SS FELODIPINE. FELODIPINE 1 U 0 10 MG QD
127356912 12735691 3 SS ERY-MAX ERYTHROMYCIN 1 Oral Y 0 500 MG TABLET TID
127356912 12735691 4 SS MICARDIS PLUS HYDROCHLOROTHIAZIDETELMISARTAN 1 12.5/80 MG U 0 QD
127356912 12735691 5 SS ISOPHANE INSULIN INSULIN NOS 1 18 + 16 IU U 0
127356912 12735691 6 SS GLUCOPHAGE METFORMIN HYDROCHLORIDE 1 U 0 1000 MG BID
127356912 12735691 7 C SIMVASTATIN. SIMVASTATIN 1 U 0 20 MG QD
127356912 12735691 8 C COUMADIN WARFARIN SODIUM 1 U 0 2.5 MG
127356912 12735691 9 C ALBYL-E ASPIRINMAGNESIUM OXIDE 1 U 0 75 MG QD
127356912 12735691 10 C NEURONTIN GABAPENTIN 1 U 0 600 MG TID

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127356912 12735691 1 Product used for unknown indication
127356912 12735691 2 Product used for unknown indication
127356912 12735691 3 Respiratory tract infection
127356912 12735691 4 Product used for unknown indication
127356912 12735691 5 Product used for unknown indication
127356912 12735691 6 Product used for unknown indication
127356912 12735691 7 Product used for unknown indication
127356912 12735691 8 Product used for unknown indication
127356912 12735691 9 Product used for unknown indication
127356912 12735691 10 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127356912 12735691 HO
127356912 12735691 LT
127356912 12735691 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
127356912 12735691 Acute kidney injury
127356912 12735691 Drug interaction
127356912 12735691 Hyperkalaemia
127356912 12735691 Hypoglycaemia
127356912 12735691 Hypotension
127356912 12735691 Hypothermia
127356912 12735691 Lactic acidosis
127356912 12735691 Sinus bradycardia

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

no results found

Therapies reported

no results found