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
7788517 8043424 F 7788517-3 20110519 20110927 20110930 EXP PHHY2011US58183 NOVARTIS PHARMACEUTICAL CORPORATION 61 YR F Y 20110929 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
7788517 1017675150 C MULTI-VITAMINS 1 ORAL 1 DF, DAILY
7788517 1017675151 C CALCIUM CARBONATE 1 ORAL 1 DF, DAILY
7788517 1017675148 PS GILENYA 1 ORAL 0.5 MG, QD 022527
7788517 1017675154 C VITAMIN D 1 ORAL 1 DF, DAILY
7788517 1017675152 C DARVOCET-N 50 1 ORAL UNK
7788517 1017675153 C VITAMIN B-12 1 ORAL 1 DF, DAILY
7788517 1017675149 C SYNTHROID 1 ORAL 1 DF, DAILY
7788517 1017675155 C PROZAC 1 ORAL 20 UG, UNK
7788517 1017675156 C BACLOFEN 1 5 MG, BID

Indications of drugs used

Event ID DRUG SEQ INDI PT
7788517 1017675148 MULTIPLE SCLEROSIS
7788517 1017675152 PAIN
7788517 1017675149 HYPOTHYROIDISM
7788517 1017675156 MUSCLE SPASTICITY

Outcome of event

Event ID OUTC COD
7788517 DS
7788517 OT

Reactions reported

Event ID PT
7788517 HEADACHE
7788517 COUGH
7788517 ABDOMINAL PAIN UPPER
7788517 JOINT SWELLING
7788517 OEDEMA PERIPHERAL
7788517 DIZZINESS
7788517 DYSPNOEA

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
7788517 1017675148 20110518 20110628 42 DAY
7788517 1017675155 20110307
7788517 1017675156 20100701 20110307 250 DAY