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
8248796 8394103 F 8248796-5 20111201 20120327 20120331 EXP PHHY2012CA002726 NOVARTIS PHARMACEUTICAL CORPORATION 51 YR F Y 20120329 MD CANADA

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
8248796 1019282950 C STEROIDS NOS 2 UNK UKN, UNK
8248796 1019282953 C FOSAMAX 1 UNK UKN, UNK
8248796 1019282949 C VITAMIN D 1 UNK UKN, UNK
8248796 1019282952 C HYDROMORPHONE HCL 1 UNK UKN, UNK
8248796 1019282956 C ALENDRONATE SODIUM 1
8248796 1019282944 PS GILENYA 1 ORAL 0.5 MG, DAILY 022527
8248796 1019282945 C DITROPAN 1 UNK UKN, UNK
8248796 1019282948 C SYNTHROID 1 UNK UKN, UNK
8248796 1019282955 C OXYBUTYNIN 1
8248796 1019282947 C CELEBREX 1 UNK UKN, UNK
8248796 1019282954 C BIOCAL D FORTE 2 UNK UKN, UNK
8248796 1019282957 C CALCIUM CARBONATE 1 UNK
8248796 1019282946 C IRBESARTAN 1 UNK UKN, UNK
8248796 1019282951 C DILAUDID 1 UNK UKN, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248796 1019282944 RELAPSING-REMITTING MULTIPLE SCLEROSIS

Outcome of event

Event ID OUTC COD
8248796 HO
8248796 DS
8248796 OT
8248796 LT

Reactions reported

Event ID PT
8248796 GRAND MAL CONVULSION
8248796 HEMIPARESIS
8248796 ATAXIA
8248796 HEADACHE
8248796 FATIGUE
8248796 LOSS OF CONSCIOUSNESS
8248796 CSF PROTEIN INCREASED
8248796 BLOOD MAGNESIUM DECREASED
8248796 CENTRAL NERVOUS SYSTEM LESION
8248796 PYREXIA
8248796 BLOOD PRESSURE INCREASED
8248796 HEPATIC ENZYME INCREASED
8248796 MUSCLE RIGIDITY
8248796 COGNITIVE DISORDER

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
8248796 1019282944 20111220 20120129 41 DAY