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CERVICOBRACHIAL SYNDROME side effect

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Chantix Side Effects Report #5463426-3
Physician from UNITED STATES reported CHANTIX problem on Sept 08, 2007. Female patient, weighting 145.1 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, fall, joint swelling, musculoskeletal pain, osteoarthritis, . CHANTIX dosage: unknown. During the same period patient was treated with VITAMINS. Patient recovered.

Chantix Side Effects Report #5418679-4
CHANTIX problem was reported by a Physician from UNITED STATES on Aug 07, 2007. Female patient, weighting 145.1 lb, was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, fall, joint swelling, musculoskeletal pain, osteoarthritis, . CHANTIX dosage: unknown. During the same period patient was treated with VITAMIN. Patient recovered.

Natalizumab Side Effects Report #5392742-9
Physician from GERMANY reported NATALIZUMAB problem on July 11, 2007. Male patient, 25 years of age, weighting 154.3 lb, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, road traffic accident, upper limb fracture, whiplash injury, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5402125-0
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, spinal osteoarthritis, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.


Natalizumab Side Effects Report #5392742-9
Physician from GERMANY reported NATALIZUMAB problem on July 11, 2007. Male patient, 25 years of age, weighting 154.3 lb, was diagnosed with multiple sclerosis and was treated with NATALIZUMAB. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, road traffic accident, upper limb fracture, whiplash injury, . NATALIZUMAB dosage: 300 MG;QM;IV. Patient was hospitalized. Patient recovered.

Avonex Side Effects Report #5402125-0
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on July 23, 2007. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, spinal osteoarthritis, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Arava Side Effects Report #5789440-6
Consumer or non-health professional from AUSTRALIA reported ARAVA problem on June 19, 2008. Female patient, 64 years of age, was treated with ARAVA. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, . ARAVA dosage: unknown. Patient recovered.

Forteo Side Effects Report #5795291-9
FORTEO problem was reported by a Physician from UNITED STATES on June 16, 2008. Female patient was diagnosed with osteoporosis and was treated with FORTEO. After drug was administered, patient experienced the following problems/side effects: cervicobrachial syndrome, spondylitis, . FORTEO dosage: unknown. During the same period patient was treated with PREDNISONE, TRENTAL, VERAPAMIL. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5537080-6
Health Professional from GERMANY reported METFORMIN problem on Dec 05, 2007. Female patient, 65 years of age, was diagnosed with type 2 diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anaemia megaloblastic, cervicobrachial syndrome, deep vein thrombosis, hyperhomocysteinaemia, vitamin b12 deficiency, . METFORMIN dosage: unknown. During the same period patient was treated with PYRIDOSTIGMINE BROMIDE, GLYBURIDE. Patient was hospitalized. Patient recovered.


Avonex Side Effects Report #5490295-8
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 04, 2007. Female patient, 63 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, non-cardiac chest pain, stress, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.

Lyrica Side Effects Report #5405416-2
Physician from AUSTRALIA reported LYRICA problem on July 25, 2007. Female patient, weighting 101.4 lb, was diagnosed with neuritis, back pain and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: bone pain, cervicobrachial syndrome, muscle spasms, neck pain, nuchal rigidity, . LYRICA dosage: unknown. During the same period patient was treated with ASPIRIN, LIPITOR, METOPROLOL SUCCINATE, NORVASC, TAMOXIFEN CITRATE, TRAMADOL. Patient recovered.

Doxil Side Effects Report #5357021-4
DOXIL problem was reported by a Health Professional from UNITED STATES on June 12, 2007. Female patient, 67 years of age, weighting 173.0 lb, was diagnosed with ovarian cancer and was treated with DOXIL. After drug was administered, patient experienced the following problems/side effects: bone graft, cervicobrachial syndrome, spinal osteoarthritis, . DOXIL dosage: 50MG/M2 Q28 DAYS IV. During the same period patient was treated with ATRASENTAN. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5320307-3
Physician from UNITED STATES reported FOSAMAX problem on Apr 30, 2007. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, depression, ear discomfort, facial pain, gastrooesophageal reflux disease, infection, joint injury, myofascial pain syndrome, . FOSAMAX dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D. Patient recovered.

Fosamax Side Effects Report #5330096-4
FOSAMAX problem was reported by a Physician from UNITED STATES on May 08, 2007. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, depression, ear discomfort, facial pain, gastrooesophageal reflux disease, infection, meniscus lesion, myofascial pain syndrome, . FOSAMAX dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D. Patient was hospitalized and became disabled. Patient recovered.


Fosamax Side Effects Report #5335173-X
Physician from UNITED STATES reported FOSAMAX problem on May 17, 2007. Female patient, 54 years of age, weighting 145.5 lb, was diagnosed with osteoporosis, osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, depression, ear discomfort, facial pain, gastrooesophageal reflux disease, infection, meniscus lesion, myofascial pain syndrome, . FOSAMAX dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D. Patient was hospitalized and became disabled. Patient recovered.

Fosamax Side Effects Report #5293856-4
FOSAMAX problem was reported by a Physician from UNITED STATES on Apr 02, 2007. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, depression, ear discomfort, facial pain, gastrooesophageal reflux disease, hyperlipidaemia, infection, insomnia, . FOSAMAX dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D. Patient recovered.

Neurontin Side Effects Report #5270290-4
Consumer or non-health professional from UNITED STATES reported NEURONTIN problem on Mar 08, 2007. Male patient, weighting 188.1 lb, was diagnosed with carpal tunnel syndrome, neuropathy peripheral, pain, ulnar nerve injury and was treated with NEURONTIN. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, completed suicide, depression, gun shot wound, injury, pain, stress, suicidal ideation, . NEURONTIN dosage: DAILY DOSE:900MG. During the same period patient was treated with BEXTRA, MEDROL, ULTRACET, CYCLOBENZAPRINE, HYDROCODONE. Patient died on 07/30/2003.

Fosamax Side Effects Report #5272717-0
FOSAMAX problem was reported by a Physician from UNITED STATES on Mar 07, 2007. Female patient, 54 years of age, was diagnosed with osteoporosis and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, cervicobrachial syndrome, depression, ear discomfort, facial pain, gastrooesophageal reflux disease, infection, joint injury, myofascial pain syndrome, . FOSAMAX dosage: unknown. During the same period patient was treated with FOSAMAX PLUS D. Patient recovered.

Fluvastatin Side Effects Report #5650753-X
Consumer or non-health professional from GERMANY reported FLUVASTATIN problem on Feb 28, 2008. Male patient, 61 years of age, was diagnosed with hypercholesterolaemia, hypertension and was treated with FLUVASTATIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, blood creatine phosphokinase increased, cervicobrachial syndrome, epicondylitis, muscle rigidity, muscle spasms, myopathy, pain, tenosynovitis, . FLUVASTATIN dosage: 20 MG, QD. During the same period patient was treated with KARVEZIDE. Patient recovered.


Fluvastatin Side Effects Report #5662654-1
FLUVASTATIN problem was reported by a Consumer or non-health professional from GERMANY on Mar 10, 2008. Male patient, 61 years of age, was diagnosed with hypercholesterolaemia, hypertension and was treated with FLUVASTATIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, blood creatine phosphokinase increased, cervicobrachial syndrome, epicondylitis, muscle rigidity, muscle spasms, myopathy, pain, tenosynovitis, . FLUVASTATIN dosage: 20 MG, QD. During the same period patient was treated with KARVEZIDE. Patient recovered.

Accutane Side Effects Report #5683903-X
Consumer or non-health professional from UNITED STATES reported ACCUTANE problem on Mar 19, 2008. Female patient, 22 years of age, weighting 190.0 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: back pain, cervicitis, cervicobrachial syndrome, chapped lips, cholelithiasis, colitis, colitis ulcerative, dry eye, dry skin, . ACCUTANE dosage: unknown. Patient was hospitalized. Patient recovered.

Seroquel Side Effects Report #5581751-2
SEROQUEL problem was reported by a Physician from UNITED STATES on Apr 10, 2007. Female patient, weighting 175.3 lb, was diagnosed with major depression and was treated with SEROQUEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, back pain, cervicobrachial syndrome, convulsion, diabetic coma, injury, intervertebral disc protrusion, limb injury, muscle strain, . SEROQUEL dosage: 25 TO 250 MG. During the same period patient was treated with ZYPREXA. Patient was hospitalized. Patient recovered.

Fosamax Side Effects Report #5584405-1
Consumer or non-health professional from UNITED STATES reported FOSAMAX problem on Dec 12, 2006. Female patient, 71 years of age, weighting 167.0 lb, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: anxiety, arthralgia, cervicobrachial syndrome, depression, foreign body trauma, joint stiffness, osteonecrosis, . FOSAMAX dosage: 70 MG/WKY/PO. Patient recovered.

Byetta Side Effects Report #5797862-2
BYETTA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 25, 2008. Female patient, 53 years of age, weighting 304.9 lb, 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 decreased, blood glucose increased, cervicobrachial syndrome, headache, nausea, vomiting, weight decreased, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, GLIPIZIDE. Patient recovered.