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
126680153 12668015 3 F 20160922 20160819 20160926 EXP PHEH2016US020439 NOVARTIS 0.00 M Y 0.00000 20160926 MD US US

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
126680153 12668015 1 PS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Unknown 20 MG, UNK U 21008 20 MG VIAL
126680153 12668015 2 SS SANDOSTATIN LAR DEPOT OCTREOTIDE ACETATE 1 Unknown 30 MG, UNK U 21008 30 MG VIAL
126680153 12668015 3 SS XANAX ALPRAZOLAM 1 Unknown 25 MG, QD (AT NIGHT) U 0 25 MG QD
126680153 12668015 4 C AMOXICILLIN. AMOXICILLIN 1 Unknown U 0
126680153 12668015 5 C ASPIRIN//ACETYLSALICYLIC ACID ASPIRIN 1 Unknown 81 MG, QD U 0 81 MG QD
126680153 12668015 6 C FINASTERIDE. FINASTERIDE 1 Unknown 5 MG, QD (AT BEDTIME) U 0 5 MG QD
126680153 12668015 7 C IRON IRON 1 Unknown 325 MG, BID U 0 325 MG BID
126680153 12668015 8 C LOPERAMIDE HCL LOPERAMIDE HYDROCHLORIDE 1 Unknown UNK UNK, PRN U 0
126680153 12668015 9 C MAGNESIUM OXIDE. MAGNESIUM OXIDE 1 Unknown 400 MG, BID U 0 400 MG BID
126680153 12668015 10 C NOVOLOG INSULIN ASPART 1 Unknown U 0
126680153 12668015 11 C OXYGEN. OXYGEN 1 Unknown UNK U 0
126680153 12668015 12 C TORASEMIDE TORSEMIDE 1 Unknown 20 MG, QD U 0 20 MG QD
126680153 12668015 13 C TAMSULOSIN TAMSULOSIN 1 Unknown UNK UNK, QD ONE AT BED TIME DAILY) U 0 CAPSULE QD

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
126680153 12668015 1 Product used for unknown indication
126680153 12668015 3 Product used for unknown indication
126680153 12668015 4 Fungal infection
126680153 12668015 5 Product used for unknown indication
126680153 12668015 6 Benign prostatic hyperplasia
126680153 12668015 7 Anaemia
126680153 12668015 8 Diarrhoea
126680153 12668015 9 Blood magnesium decreased
126680153 12668015 10 Product used for unknown indication
126680153 12668015 11 Product used for unknown indication
126680153 12668015 12 Blood pressure increased
126680153 12668015 13 Benign prostatic hyperplasia

Outcome of event

Event ID CASEID OUTC COD
126680153 12668015 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
126680153 12668015 Constipation
126680153 12668015 Diabetes mellitus
126680153 12668015 Dyspnoea
126680153 12668015 Hepatic neoplasm
126680153 12668015 Injection site mass
126680153 12668015 Injection site pain
126680153 12668015 Somnolence
126680153 12668015 Weight decreased

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

no results found

Therapies reported

no results found