The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
119401492 11940149 2 F 2007 20160628 20160122 20160705 EXP US-TEIKOKU PHARMA USA-TPU2016-00042 TEIKOKU 0.00 F Y 64.01000 KG 20160705 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
119401492 11940149 1 PS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 2 SS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 3 SS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 4 SS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 5 SS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 6 SS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 7 SS LIDODERM LIDOCAINE 1 94248 20612
119401492 11940149 8 SS steroid injection UNSPECIFIED INGREDIENT 1 180 AND 40MG 0
119401492 11940149 9 SS PREDNISONE. PREDNISONE 1 0
119401492 11940149 10 SS PREDNISONE. PREDNISONE 1 0
119401492 11940149 11 C SYNTHROID LEVOTHYROXINE SODIUM 1 0
119401492 11940149 12 C CALCIUM D CALCIUMVITAMIN D 1 0
119401492 11940149 13 C XANAX ALPRAZOLAM 1 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
119401492 11940149 1 Ulnar nerve injury
119401492 11940149 2 Musculoskeletal pain
119401492 11940149 3 Procedural pain
119401492 11940149 4 Pain in extremity
119401492 11940149 5 Small fibre neuropathy
119401492 11940149 6 Back pain
119401492 11940149 7 Muscle atrophy
119401492 11940149 8 Pain management
119401492 11940149 9 Bronchitis
119401492 11940149 10 Upper respiratory tract infection
119401492 11940149 11 Thyroidectomy
119401492 11940149 12 Hypocalcaemia
119401492 11940149 13 Sleep disorder

Outcome of event

Event ID CASEID OUTC COD
119401492 11940149 OT
119401492 11940149 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
119401492 11940149 Accident
119401492 11940149 Alopecia
119401492 11940149 Anger
119401492 11940149 Arthralgia
119401492 11940149 Bronchitis
119401492 11940149 Burning sensation
119401492 11940149 Cerebral disorder
119401492 11940149 Dysphagia
119401492 11940149 Fat tissue decreased
119401492 11940149 Herpes simplex
119401492 11940149 Incorrect drug administration duration
119401492 11940149 Limb injury
119401492 11940149 Logorrhoea
119401492 11940149 Memory impairment
119401492 11940149 Menopause
119401492 11940149 Muscle atrophy
119401492 11940149 Oral pain
119401492 11940149 Oversensing
119401492 11940149 Repetitive speech
119401492 11940149 Restlessness
119401492 11940149 Retching
119401492 11940149 Road traffic accident
119401492 11940149 Rotator cuff repair
119401492 11940149 Sciatica
119401492 11940149 Skin atrophy
119401492 11940149 Small fibre neuropathy
119401492 11940149 Tremor
119401492 11940149 Upper respiratory tract infection
119401492 11940149 Vision blurred
119401492 11940149 Weight decreased
119401492 11940149 Wound

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

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
119401492 11940149 1 2009 0
119401492 11940149 8 2005 2013 0
119401492 11940149 9 201505 0
119401492 11940149 11 1969 0
119401492 11940149 12 1969 0