The Safety Rates Drug Report

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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
8248780 8486003 I 8248780-1 20120205 20120323 20120331 EXP PHEH2012US006624 NOVARTIS PHARMACEUTICAL CORPORATION 49 YR M Y 20120331 MD 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
8248780 1019282860 C HYTONE 1 TOPICAL UNK UKN, UNK
8248780 1019282855 C CAPSAICIN 2 TOPICAL UNK UKN, UNK
8248780 1019282856 C FLEXERIL 1 ORAL 1 DF, PRN
8248780 1019282857 C VALIUM 1 ORAL 1 DF, PRN
8248780 1019282859 C VITAMIN D 1 ORAL UNK UKN, UNK
8248780 1019282864 C SONATA 1 ORAL 1 DF, QD
8248780 1019282865 C RECLAST 1 INTRAVENOUS UNK UKN, UNK
8248780 1019282852 C NUVIGIL 1 ORAL 150 MG, QD
8248780 1019282854 C CALTRATE 600 + VITAMIN D 2 ORAL 1 DF, BID
8248780 1019282858 C COLACE 2 ORAL 1 DF, BID
8248780 1019282853 C ASCORBIC ACID 1 ORAL UNK UKN, UNK
8248780 1019282863 C DETROL 1 ORAL 1 DF, QD
8248780 1019282851 PS GILENYA 1 ORAL 0.5 MG, QD 022527
8248780 1019282861 C MS CONTIN 1 ORAL 1 DF, BID
8248780 1019282862 C PERCOCET 1 ORAL UNK UKN, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248780 1019282851 MULTIPLE SCLEROSIS

Outcome of event

Event ID OUTC COD
8248780 DE

Reactions reported

Event ID PT
8248780 DEATH

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
8248780 1019282851 20110929