The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASE I F COD FOLL SEQ IMAGE EVENT DT MFR DT FDA DT REPT COD MFR NUM MFR SNDR AGE AGE COD GNDR COD E SUB WT WT COD REPT DT OCCP COD DEATH DT TO MFR CONFID REPORTER COUNTRY
8248795 8327125 F 8248795-3 20111008 20120323 20120331 EXP PHEH2012US000691 NOVARTIS PHARMACEUTICAL CORPORATION 48 YR M Y 20120329 OT UNITED STATES

Drug(s) used by person

Event ID DRUG SEQ ROLE COD DRUGNAME VAL VBM ROUTE DOSE VBM DECHAL RECHAL LOT NUM EXP DT NDA NUM
8248795 1019282934 SS ALPRAZOLAM 1 UNK UKN, OT
8248795 1019282938 C TIZANIDINE HCL 1 4 MG, UNK
8248795 1019282940 C IBUPROFEN 1
8248795 1019282935 SS HEROIN 2 UNK UKN, OT
8248795 1019282932 PS GILENYA 1 ORAL 0.5 MG, QD 022527
8248795 1019282937 C GABAPENTIN 1 800 MG, UNK
8248795 1019282939 C TAMSULOSIN HCL 1 0.4 MG, UNK
8248795 1019282933 SS CYCLOBENZAPRINE HCL 1 UNK UKN, OT
8248795 1019282941 C VITAMIN D 1
8248795 1019282936 C LISINOPRIL 1 10 MG, UNK
8248795 1019282942 C PRILOSEC 1 20 MG/DAY
8248795 1019282943 C FLOMAX 1 0.4 MG, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248795 1019282932 MULTIPLE SCLEROSIS
8248795 1019282942 GASTROOESOPHAGEAL REFLUX DISEASE
8248795 1019282943 POLLAKIURIA

Outcome of event

Event ID OUTC COD
8248795 DE
8248795 OT

Reactions reported

Event ID PT
8248795 LEFT VENTRICULAR HYPERTROPHY
8248795 MUSCLE SPASMS
8248795 CARDIOMEGALY
8248795 PAIN IN EXTREMITY
8248795 BLADDER OUTLET OBSTRUCTION
8248795 NEUROGENIC BLADDER
8248795 POLLAKIURIA
8248795 TOXICITY TO VARIOUS AGENTS
8248795 HYPERTENSIVE HEART DISEASE
8248795 DRUG ABUSE

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

no results found

Therapies reported

Event ID DRUG SEQ START DT END DT DUR DUR COD
8248795 1019282932 20101230
8248795 1019282943 20101117