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FOOT DEFORMITY side effect

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Rebif Side Effects Report #5593351-9
Consumer or non-health professional from UNITED STATES reported REBIF problem on Jan 02, 2008. Female patient, 57 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: foot deformity, localised infection, no therapeutic response, osteomyelitis, ulcer, . REBIF dosage: unknown. During the same period patient was treated with ACCUPRIL, DYNACIRC CR, CYMBALTA, TRAMADOL, PREVACID, LYRICA. Patient was hospitalized. Patient recovered.

Fentanyl Side Effects Report #5608753-1
FENTANYL TRANSDERMAL SYSTEM problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 21, 2008. Male patient, weighting 180.0 lb, was diagnosed with neck pain, back pain and was treated with FENTANYL TRANSDERMAL SYSTEM. After drug was administered, patient experienced the following problems/side effects: foot deformity, weight increased, . FENTANYL TRANSDERMAL SYSTEM dosage: unknown. During the same period patient was treated with FENTANYL TRANSDERMAL SYSTEM, NORCO. Patient recovered.

Rebif Side Effects Report #5568542-3
Consumer or non-health professional from UNITED STATES reported REBIF problem on Dec 05, 2007. Female patient, 57 years of age, was diagnosed with multiple sclerosis and was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: foot deformity, localised infection, no therapeutic response, osteomyelitis, ulcer, . REBIF dosage: unknown. During the same period patient was treated with ACCUPRIL, DYNACIRC CR, CYMBALTA, TRAMADOL, PREVACID, LYRICA. Patient was hospitalized. Patient recovered.

Effexor Side Effects Report #5586485-6
EFFEXOR problem was reported by a Physician from UNITED STATES on June 05, 2007. Female patient was diagnosed with major depression and was treated with EFFEXOR. After drug was administered, patient experienced the following problems/side effects: foot deformity, pain in extremity, . EFFEXOR dosage: unknown. Patient recovered.


Forteo Side Effects Report #5482739-2
Consumer or non-health professional from FRANCE reported FORTEO problem on Oct 05, 2007. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: foot deformity, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5498158-9
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 15, 2007. Female patient, weighting 135.1 lb, was diagnosed with psoriatic arthropathy, rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: foot deformity, limb deformity, malaise, nasopharyngitis, pneumonia, . HUMIRA dosage: unknown. Patient was hospitalized. Patient recovered.

Levemir Side Effects Report #5504326-X
Consumer or non-health professional from UNITED STATES reported LEVEMIR problem on Sept 17, 2007. Female patient, 68 years of age, was diagnosed with type 2 diabetes mellitus and was treated with LEVEMIR. After drug was administered, patient experienced the following problems/side effects: foot deformity, muscle spasms, musculoskeletal pain, . LEVEMIR dosage: unknown. During the same period patient was treated with DIOVAN, NORVASC, TOPROL, GLUCOTROL. Patient recovered.

Coreg Side Effects Report #5453814-3
COREG problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 12, 2007. Female patient, 69 years of age, weighting 151.2 lb, was treated with COREG. After drug was administered, patient experienced the following problems/side effects: foot deformity, insomnia, muscle spasms, pain in extremity, peripheral ischaemia, . COREG dosage: 12.5MG TWICE PER DAY. During the same period patient was treated with COREG CR, PRAVASTATIN, FUROSEMIDE, OMEPRAZOLE, ASPIRIN, MAGNESIUM SULPHATE, ONE A DAY VITAMIN, CALCIUM. Patient recovered.

Humira Side Effects Report #5385924-3
Consumer or non-health professional from BELGIUM reported HUMIRA problem on July 04, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis, prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: foot deformity, wound infection, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, BEVIPLEX, CALCIUM CHLORIDE. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5402211-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 19, 2007. Female patient, 64 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: foot deformity, multiple sclerosis relapse, weight decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5385924-3
Consumer or non-health professional from BELGIUM reported HUMIRA problem on July 04, 2007. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis, prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: foot deformity, wound infection, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, BEVIPLEX, CALCIUM CHLORIDE. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5402211-5
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 19, 2007. Female patient, 64 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: foot deformity, multiple sclerosis relapse, weight decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5774887-4
Consumer or non-health professional from FRANCE reported FORTEO problem on June 06, 2008. Female patient, 72 years of age, was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: foot deformity, osteitis, pain in extremity, . FORTEO dosage: unknown. Patient was hospitalized. Patient recovered.

Forteo Side Effects Report #5728826-2
FORTEO problem was reported by a Physician from FRANCE on Apr 28, 2008. Female patient, 77 years of age, weighting 109.1 lb, was diagnosed with osteoporosis, hypertension and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: foot deformity, thrombophlebitis superficial, . FORTEO dosage: unknown. During the same period patient was treated with PRACTAZIN. Patient was hospitalized. Patient recovered.


Humira Side Effects Report #5740443-7
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on May 08, 2008. Female patient, weighting 240.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: foot deformity, nerve injury, oedema peripheral, pain in extremity, . HUMIRA dosage: unknown. During the same period patient was treated with CELECOXIB, ACETAMINOPHEN, ADVIL. Patient recovered.

Cerezyme Side Effects Report #5724207-6
CEREZYME problem was reported by a Physician from GREECE on Apr 11, 2008. Female patient was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: foot deformity, . CEREZYME dosage: unknown. Patient recovered.

Lipitor Side Effects Report #5652081-5
Physician from UNITED STATES reported LIPITOR problem on Feb 26, 2008. Female patient, weighting 158.1 lb, was diagnosed with hyperlipidaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: asthenia, foot deformity, fracture, neuropathy peripheral, . LIPITOR dosage: TEXT:BETWEEN 40 AND 80 MG. During the same period patient was treated with LAMICTAL, TRILEPTAL. Patient recovered.

Humira Side Effects Report #5667713-5
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 30, 2008. Female patient, 63 years of age, weighting 175.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bursitis, foot deformity, joint swelling, . HUMIRA dosage: unknown. During the same period patient was treated with HYDROXYCHLOROQUINE PHOSPHATE. Patient recovered.

Humira Side Effects Report #5478711-9
Consumer or non-health professional from BRAZIL reported HUMIRA problem on Sept 27, 2007. Female patient, weighting 123.5 lb, was diagnosed with rheumatoid arthritis, pain, hypertension, cardiac failure and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: anaemia, foot deformity, weight increased, . HUMIRA dosage: unknown. During the same period patient was treated with CHLORTHALIDONE. Patient was hospitalized. Patient recovered.


Seroquel Side Effects Report #5460537-3
SEROQUEL problem was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2007. Female patient, 19 years of age, was diagnosed with bipolar disorder and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: dyskinesia, foot deformity, muscle twitching, muscular weakness, vision blurred, . SEROQUEL dosage: unknown. During the same period patient was treated with LAMICTAL, INHALERS, ADVAIR DISKUS, PROAIR HFA, VENTOLIN HFA. Patient recovered.

Lipitor Side Effects Report #5413108-9
Consumer or non-health professional from UNITED STATES reported LIPITOR problem on Aug 01, 2007. Female patient, weighting 164.3 lb, was diagnosed with blood cholesterol increased and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: acquired claw toe, foot deformity, muscle spasms, pain in extremity, tendonitis, . LIPITOR dosage: unknown. During the same period patient was treated with PREMPRO, CALCIUM CHLORIDE. Patient recovered.

Keppra Side Effects Report #5764389-3
KEPPRA problem was reported by a Physician from UNITED STATES on May 20, 2008. Female patient was diagnosed with convulsion and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: foetal growth retardation, foot deformity, haemangioma, premature baby, . KEPPRA dosage: 3000 MG /D TRP. During the same period patient was treated with LAMICTAL, PROCARDIA, FOLIC ACID, VITAMIN, BETAMETHASONE. Patient recovered.

Avonex Side Effects Report #5774572-9
Physician from UNITED STATES reported AVONEX problem on June 03, 2008. Female patient was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: congenital anomaly, foot deformity, . AVONEX dosage: unknown. Patient recovered.

Keppra Side Effects Report #5797495-8
KEPPRA problem was reported by a Physician from UNITED STATES on June 16, 2008. Female patient was diagnosed with convulsion and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: foetal growth retardation, foot deformity, haemangioma, premature baby, . KEPPRA dosage: 3000 MG/ D TRP. During the same period patient was treated with LAMICTAL, PROCARDIA, FOLIC ACID, VITAMIN, BETAMETHASONE. Patient recovered.

Cerezyme Side Effects Report #5741395-6
Physician from GREECE reported CEREZYME problem on Apr 30, 2008. Female patient, child 12 years of age, was diagnosed with gaucher's disease and was treated with CEREZYME. After drug was administered, patient experienced the following problems/side effects: condition aggravated, foot deformity, . CEREZYME dosage: 60 MG/KG, Q2W, INTRAVENOUS. Patient recovered.

Keppra Side Effects Report #5752022-6
KEPPRA problem was reported by a Physician from UNITED STATES on May 13, 2008. Female patient was diagnosed with convulsion and was treated with KEPPRA. After drug was administered, patient experienced the following problems/side effects: foetal growth retardation, foot deformity, haemangioma, premature baby, . KEPPRA dosage: 3000 MG/ D TRP. During the same period patient was treated with LAMICTAL, PROCARDIA, FOLIC ACID, VITAMIN, BETAMETHASONE. Patient recovered.

Forteo Side Effects Report #5646900-6
Consumer or non-health professional from FRANCE reported FORTEO problem on Feb 25, 2008. Female patient, 77 years of age, was diagnosed with osteoporosis, hypertension and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: condition aggravated, fatigue, foot deformity, thrombophlebitis, . FORTEO dosage: unknown. During the same period patient was treated with PRACTAZIN. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5583417-1
LYRICA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 26, 2007. Female patient, weighting 154.1 lb, was diagnosed with headache and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: fall, feeling drunk, foot deformity, . LYRICA dosage: unknown. During the same period patient was treated with METOPROLOL, SIMVASTATIN, VITAMINS, NEXIUM, VITAMIN B CAP, VITAMIN D, CALCIUM, MAGNESIUM. Patient recovered.

Remicade Side Effects Report #5588309-X
Consumer or non-health professional from UNITED STATES reported REMICADE problem on Jan 04, 2008. Female patient, weighting 183.0 lb, was diagnosed with rheumatoid arthritis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: dysgeusia, finger deformity, foot deformity, malaise, oedema peripheral, pharyngolaryngeal pain, weight decreased, . REMICADE dosage: unknown. During the same period patient was treated with PREDNISONE, METHOTREXATE. Patient was hospitalized. Patient recovered.

Byetta Side Effects Report #5477242-X
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 27, 2007. Female patient was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased, bunion, foot deformity, visual acuity reduced, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, AVANDIA. Patient was hospitalized. Patient recovered.

Actos Side Effects Report #5410419-8
Physician from FRANCE reported ACTOS problem on July 30, 2007. Female patient, 58 years of age, was diagnosed with type 2 diabetes mellitus and was treated with ACTOS. After drug was administered, patient experienced the following problems/side effects: diabetic neuropathy, erythema, foot deformity, foot fracture, hypoaesthesia, inflammation, osteolysis, . ACTOS dosage: 45 MG (45 MG, 1 IN 1 D) ORAL. During the same period patient was treated with GLYBURIDE, LUDIOMIL, HAVLANE, EFFEXOR, LESCOL, GINKORT, CALCIDOSE D. Patient recovered.

Humira Side Effects Report #5756117-2
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on May 23, 2008. Female patient, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bursitis, cellulitis, foot deformity, inflammation of wound, joint instability, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, PREDNISOLONE, OMEPRAZOLE, OYSTER SHELL CALCIUM WITH VITAMIN D. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5777649-7
Consumer or non-health professional from GERMANY reported HUMIRA problem on June 09, 2008. Female patient, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bursitis, cellulitis, foot deformity, inflammation of wound, joint instability, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, PREDNISOLONE, OMEPRAZOLE, OYSTER SHELL CALCIUM WITH VITAMIN D. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5727697-8
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Apr 25, 2008. Female patient, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bursitis, cellulitis, foot deformity, inflammation of wound, joint instability, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5740750-8
Consumer or non-health professional from GERMANY reported HUMIRA problem on May 08, 2008. Female patient, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bursitis, cellulitis, foot deformity, inflammation of wound, joint instability, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Humira Side Effects Report #5703079-X
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on Apr 02, 2008. Female patient, weighting 145.5 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bursitis, cellulitis, foot deformity, inflammation of wound, joint instability, . HUMIRA dosage: unknown. During the same period patient was treated with LEFLUNOMIDE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Clonazepam Side Effects Report #5269722-7
Consumer or non-health professional from FRANCE reported CLONAZEPAM problem on Mar 08, 2007. Female patient, 32 years of age, was treated with CLONAZEPAM. After drug was administered, patient experienced the following problems/side effects: abortion induced, dysmorphism, foot deformity, syndactyly, . CLONAZEPAM dosage: unknown. During the same period patient was treated with SUBUTEX, PROZAC, SKENAN, METHADONE. Patient was hospitalized. Patient died.