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
1024069417 10240694 17 F 20101019 20160616 20140617 20160630 EXP US-ACORDA-ACO_26425_2011 ACORDA 84.51 YR F Y 57.60000 KG 20160630 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
1024069417 10240694 1 PS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, Q 12 HRS 22250 10 MG TABLET Q12H
1024069417 10240694 2 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, QD 22250 10 MG TABLET QD
1024069417 10240694 3 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET BID
1024069417 10240694 4 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, QD 22250 10 MG TABLET QD
1024069417 10240694 5 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET BID
1024069417 10240694 6 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET Q12H
1024069417 10240694 7 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET BID
1024069417 10240694 8 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, BID 22250 10 MG TABLET BID
1024069417 10240694 9 SS AMPYRA DALFAMPRIDINE 1 Oral 10 MG, QD 22250 10 MG TABLET QD
1024069417 10240694 10 C SYNTHROID LEVOTHYROXINE SODIUM 1 Oral 112 ?G, QD U 0 112 UG QD
1024069417 10240694 11 C BACLOFEN. BACLOFEN 1 Oral 10 MG, BID U 0 10 MG BID
1024069417 10240694 12 C LASIX FUROSEMIDE 1 U 0
1024069417 10240694 13 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown 1000 ?G, QD U 0 1000 UG QD
1024069417 10240694 14 C VITAMIN B12 CYANOCOBALAMIN 1 Unknown 500 ?G, UNK U 0 500 UG
1024069417 10240694 15 C CALTRATE WITH VITAMIN D CALCIUM CARBONATECHOLECALCIFEROL 1 1 DF, QD U 0 1 DF QD
1024069417 10240694 16 C Centrum silver MINERALSVITAMINS 1 UNK U 0
1024069417 10240694 17 C VITAMIN D CHOLECALCIFEROL 1 Unknown 5000 UNK, UNK U 0 5000 IU
1024069417 10240694 18 C VITAMIN D CHOLECALCIFEROL 1 Unknown 1000 IU, UNK U 0 1000 IU
1024069417 10240694 19 C Potassium POTASSIUM 1 UNK U 0
1024069417 10240694 20 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 Unknown 115 ?G, UNK U 0 115 UG
1024069417 10240694 21 C LEVOTHYROXINE SODIUM. LEVOTHYROXINE SODIUM 1 112 ?G, UNK U 0 112 UG
1024069417 10240694 22 C ECOTRIN ASPIRIN 1 325 MG, UNK U 0 325 MG
1024069417 10240694 23 C ECOTRIN ASPIRIN 1 Unknown 81 MG, UNK U 0 81 MG
1024069417 10240694 24 C ASPIRIN. ASPIRIN 1 Oral 325 MG, QD U 0 325 MG QD
1024069417 10240694 25 C DITROPAN XL OXYBUTYNIN CHLORIDE 1 Unknown 5MG, 1 TAB QD U 0
1024069417 10240694 26 C LEVOTHROID LEVOTHYROXINE SODIUM 1 Unknown 113 ?G, UNK U 0 113 UG

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
1024069417 10240694 1 Gait disturbance
1024069417 10240694 2 Asthenia
1024069417 10240694 3 Dysstasia
1024069417 10240694 4 Asthenia
1024069417 10240694 10 Product used for unknown indication
1024069417 10240694 11 Muscle spasms
1024069417 10240694 12 Product used for unknown indication
1024069417 10240694 13 Product used for unknown indication
1024069417 10240694 15 Product used for unknown indication
1024069417 10240694 16 Product used for unknown indication
1024069417 10240694 17 Product used for unknown indication
1024069417 10240694 19 Product used for unknown indication
1024069417 10240694 20 Product used for unknown indication
1024069417 10240694 22 Product used for unknown indication
1024069417 10240694 24 Product used for unknown indication
1024069417 10240694 25 Product used for unknown indication
1024069417 10240694 26 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
1024069417 10240694 OT
1024069417 10240694 HO
1024069417 10240694 DS

Reactions reported

Event ID CASEID DRUG REC ACT PT
1024069417 10240694 Asthenia
1024069417 10240694 Back pain
1024069417 10240694 Bedridden
1024069417 10240694 Burning sensation
1024069417 10240694 Compression fracture
1024069417 10240694 Constipation
1024069417 10240694 Cough
1024069417 10240694 Cystitis
1024069417 10240694 Cystitis klebsiella
1024069417 10240694 Depression
1024069417 10240694 Dyskinesia
1024069417 10240694 Dysstasia
1024069417 10240694 Escherichia infection
1024069417 10240694 Gastrooesophageal reflux disease
1024069417 10240694 Headache
1024069417 10240694 Hypoaesthesia
1024069417 10240694 Inappropriate schedule of drug administration
1024069417 10240694 Insomnia
1024069417 10240694 Joint contracture
1024069417 10240694 Kidney infection
1024069417 10240694 Lower limb fracture
1024069417 10240694 Lumbar spinal stenosis
1024069417 10240694 Muscle spasms
1024069417 10240694 Muscular weakness
1024069417 10240694 Nephrolithiasis
1024069417 10240694 Oedema
1024069417 10240694 Off label use
1024069417 10240694 Osteoporosis
1024069417 10240694 Pain in extremity
1024069417 10240694 Paraesthesia
1024069417 10240694 Paranoia
1024069417 10240694 Pruritus
1024069417 10240694 Pruritus generalised
1024069417 10240694 Psychotic disorder
1024069417 10240694 Pulmonary embolism
1024069417 10240694 Sepsis
1024069417 10240694 Spinal fracture
1024069417 10240694 Stress fracture
1024069417 10240694 Therapeutic response unexpected
1024069417 10240694 Therapy cessation
1024069417 10240694 Urethral disorder
1024069417 10240694 Urinary tract infection

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
1024069417 10240694 1 20100712 0
1024069417 10240694 2 20110608 0
1024069417 10240694 4 20120926 0
1024069417 10240694 5 2012 0
1024069417 10240694 6 20120524 0
1024069417 10240694 7 20130524 201508 0
1024069417 10240694 8 20150901 0