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
8248773 7742982 F 8248773-4 20110712 20120327 20120331 EXP PHEH2010US01802 NOVARTIS PHARMACEUTICAL CORPORATION 43 YR F Y 20120330 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
8248773 1019282840 C MULTI-VITAMINS 1 UNK UKN, UNK
8248773 1019282839 C STEROIDS NOS 2 UNK UKN, UNK
8248773 1019282834 C NEURONTIN 1 400 MG, TID
8248773 1019282835 C ACETAMINOPHEN 1 UNK UKN, UNK
8248773 1019282836 C M.V.I. 1 1 DF, QD
8248773 1019282837 C VITAMIN B-12 1 2500 U, QD
8248773 1019282841 C BACLOFEN 1 ORAL 10 MG, TID
8248773 1019282831 PS EXTAVIA 1 SUBCUTANEOUS 0.25 MG, QOD
8248773 1019282832 SS LYRICA 1 ORAL 100 MG, BID
8248773 1019282833 C IBUPROFEN 1 600 MG, PRN
8248773 1019282838 C ACETAMINOPHEN 1 UNK UKN, UNK

Indications of drugs used

Event ID DRUG SEQ INDI PT
8248773 1019282841 MUSCLE SPASTICITY
8248773 1019282831 MULTIPLE SCLEROSIS
8248773 1019282832 NEURALGIA
8248773 1019282833 PAIN

Outcome of event

Event ID OUTC COD
8248773 DS
8248773 OT

Reactions reported

Event ID PT
8248773 MENISCUS LESION
8248773 DYSPHAGIA
8248773 SKIN TIGHTNESS
8248773 BURNING SENSATION
8248773 INJECTION SITE PAIN
8248773 DIZZINESS
8248773 SWOLLEN TONGUE
8248773 FATIGUE
8248773 GAIT DISTURBANCE
8248773 MYALGIA
8248773 ASPARTATE AMINOTRANSFERASE INCREASED
8248773 PAIN
8248773 MULTIPLE SCLEROSIS RELAPSE
8248773 INFLUENZA LIKE ILLNESS
8248773 ALOPECIA
8248773 BLOOD ALKALINE PHOSPHATASE INCREASED
8248773 ASTHENIA

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
8248773 1019282831 20100128
8248773 1019282832 20110712 20110817 37 DAY