JOINT RANGE OF MOTION DECREASED side effect
What is JOINT RANGE OF MOTION DECREASED ?Drugs associated with JOINT RANGE OF MOTION DECREASED
ACCUTANE ACTONEL ARIMIDEX AVANDIA AVONEX BETASERON BOTOX CHANTIX CIPROFLOXACIN ENBREL FOSAMAX GADOLINIUM HUMIRA MIRENA OMNISCAN PACERONE RECLAST REMICADE RENAGEL SPIRIVA ZOCOR ZOMETAJOINT RANGE OF MOTION DECREASED : Botox Side Effects Report #5663399-4
Consumer or non-health professional from UNITED KINGDOM reported BOTOX problem on Mar 07, 2008. Female patient was diagnosed with cerebral palsy and was treated with BOTOX. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, . BOTOX dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5667231-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 14, 2008. Female patient, weighting 100.1 lb, was diagnosed with crohn's disease, mineral supplementation, vitamin supplementation and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, musculoskeletal stiffness, neck pain, nerve compression, . HUMIRA dosage: unknown. During the same period patient was treated with ENDACORT, CALCIUM, FOLIC ACID. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Spiriva Side Effects Report #5602892-7
Physician from UNITED STATES reported SPIRIVA problem on Jan 03, 2008. Female patient, 61 years of age, weighting 119.0 lb, was diagnosed with chronic obstructive pulmonary disease and was treated with SPIRIVA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, oedema peripheral, skin tightness, . SPIRIVA dosage: unknown. During the same period patient was treated with ALBUTEROL, ADVAIR DISKUS, PREMPRO. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Enbrel Side Effects Report #5545184-7
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 16, 2007. Female patient was diagnosed with psoriatic arthropathy, psoriasis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, pain in extremity, . ENBREL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Ciprofloxacin Side Effects Report #5549355-5
Health Professional from SPAIN reported CIPROFLOXACIN problem on Nov 30, 2007. Female patient, 67 years of age, was diagnosed with urinary tract infection and was treated with CIPROFLOXACIN. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, tendon pain, . CIPROFLOXACIN dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Enbrel Side Effects Report #5550009-X
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 20, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, pain, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Enbrel Side Effects Report #5556343-1
Physician from UNITED STATES reported ENBREL problem on Sept 10, 2007. Female patient was diagnosed with juvenile arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, joint swelling, musculoskeletal stiffness, rash, swelling face, . ENBREL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Avonex Side Effects Report #5567876-6
AVONEX problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Female patient, 50 years of age, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, mobility decreased, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Avandia Side Effects Report #5452883-4
Consumer or non-health professional from UNITED STATES reported AVANDIA problem on Sept 11, 2007. Female patient, 60 years of age, was diagnosed with type 2 diabetes mellitus and was treated with AVANDIA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, muscle tightness, myocardial infarction, . AVANDIA dosage: 8MG PER DAY. During the same period patient was treated with GLUCOPHAGE, SYNTHROID, PRILOSEC. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Renagel Side Effects Report #5379948-X
RENAGEL problem was reported by a Physician from TURKEY on June 20, 2007. Male patient, 26 years of age, weighting 189.6 lb, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, polyarthritis, . RENAGEL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Renagel Side Effects Report #5398346-6
Physician from TURKEY reported RENAGEL problem on July 10, 2007. Male patient, 62 years of age, weighting 136.7 lb, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, leukocytosis, polyarthritis, . RENAGEL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5399623-5
HUMIRA problem was reported by a Consumer or non-health professional from GERMANY on July 17, 2007. Female patient, 37 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, rash papular, rash pruritic, . HUMIRA dosage: unknown. During the same period patient was treated with RITUXIMAB, METHOTREXATE, AZATHIOPRINE. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Renagel Side Effects Report #5379948-X
Physician from TURKEY reported RENAGEL problem on June 20, 2007. Male patient, 26 years of age, weighting 189.6 lb, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, polyarthritis, . RENAGEL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Renagel Side Effects Report #5398346-6
RENAGEL problem was reported by a Physician from TURKEY on July 10, 2007. Male patient, 62 years of age, weighting 136.7 lb, was diagnosed with hyperphosphataemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, leukocytosis, polyarthritis, . RENAGEL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5399623-5
Consumer or non-health professional from GERMANY reported HUMIRA problem on July 17, 2007. Female patient, 37 years of age, was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, rash papular, rash pruritic, . HUMIRA dosage: unknown. During the same period patient was treated with RITUXIMAB, METHOTREXATE, AZATHIOPRINE. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Remicade Side Effects Report #5662984-3
REMICADE problem was reported by a Health Professional from SPAIN on Mar 04, 2008. Female patient, 27 years of age, weighting 132.3 lb, was diagnosed with psoriasis and was treated with REMICADE. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, . REMICADE dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5666388-9
Physician from UNITED STATES reported HUMIRA problem on Dec 17, 2007. Male patient, weighting 175.2 lb, was diagnosed with rheumatoid arthritis, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, joint range of motion decreased, muscle disorder, muscular weakness, neck pain, tinnitus, . HUMIRA dosage: unknown. During the same period patient was treated with CELECOXIB, HYDROXYCHLOROQUINE PHOSPHATE, FOLIC ACID, PREDNISONE, ATENOLOL, VICODIN. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5666779-6
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 27, 2007. Female patient, weighting 174.2 lb, was diagnosed with ankylosing spondylitis, rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, . HUMIRA dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5668166-3
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 15, 2008. Female patient, weighting 187.2 lb, was diagnosed with rheumatoid arthritis, psoriatic arthropathy, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, joint swelling, oedema peripheral, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, TYLOX. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Zocor Side Effects Report #5615230-0
ZOCOR problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 05, 2008. Female patient, 60 years of age, weighting 180.0 lb, was treated with ZOCOR. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, joint range of motion decreased, pain in extremity, . ZOCOR dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Reclast Side Effects Report #5615275-0
Physician from UNITED STATES reported RECLAST problem on Jan 30, 2008. Female patient was treated with RECLAST. After drug was administered, patient experienced the following problems/side effects: arthritis infective, joint range of motion decreased, joint swelling, joint warmth, . RECLAST dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Enbrel Side Effects Report #5552833-6
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on June 25, 2007. Female patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: gait disturbance, joint range of motion decreased, rheumatoid arthritis, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Enbrel Side Effects Report #5561504-1
Consumer or non-health professional from UNITED STATES reported ENBREL problem on Oct 17, 2007. Male patient was diagnosed with rheumatoid arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, . ENBREL dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Arimidex Side Effects Report #5521729-8
ARIMIDEX problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 14, 2007. Female patient, 76 years of age, weighting 125.0 lb, was diagnosed with ovarian cancer and was treated with ARIMIDEX. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, malaise, musculoskeletal pain, myalgia, ovarian cancer, pain in extremity, pain in jaw, toothache, . ARIMIDEX dosage: unknown. During the same period patient was treated with PREDNISONE, NEXIUM, METOPROLOL. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Omniscan Side Effects Report #5493866-8
Physician from UNITED STATES reported OMNISCAN problem on Oct 08, 2007. Male patient, 37 years of age, was diagnosed with renal failure chronic and was treated with OMNISCAN. After drug was administered, patient experienced the following problems/side effects: abasia, joint range of motion decreased, nephrogenic systemic fibrosis, oedema, pain in extremity, . OMNISCAN dosage: 1 ML/5 KG, SINGLE DOSE, I.V.. During the same period patient was treated with VITAMIN K ANTAGONIST. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Chantix Side Effects Report #5451694-3
CHANTIX problem was reported by a Physician from UNITED STATES on Sept 04, 2007. Female patient was diagnosed with tobacco abuse and was treated with CHANTIX. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, joint range of motion decreased, urticaria, . CHANTIX dosage: unknown. During the same period patient was treated with ERYTHROMYCIN. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Zometa Side Effects Report #5424664-9
Consumer or non-health professional from GERMANY reported ZOMETA problem on Aug 21, 2007. Female patient was diagnosed with metastases to bone and was treated with ZOMETA. After drug was administered, patient experienced the following problems/side effects: biopsy, joint range of motion decreased, joint swelling, joint warmth, nuclear magnetic resonance imaging normal, pain in extremity, . ZOMETA dosage: 4 MG, QMO. During the same period patient was treated with NEXAVAR. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Pacerone Side Effects Report #5424765-5
PACERONE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 03, 2007. Male patient, 68 years of age, was diagnosed with atrial fibrillation and was treated with PACERONE. After drug was administered, patient experienced the following problems/side effects: impaired work ability, joint range of motion decreased, malaise, peripheral nerve lesion, tremor, . PACERONE dosage: 200 MG, QD, PO. During the same period patient was treated with HYDROCODONE WITH ACETAMINOPHEN, EFFEXOR, PREDNISOONE, ATACAND, FISH OIL, VITAMIN B CAP, OXYGEN. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Betaseron Side Effects Report #5377582-9
Consumer or non-health professional from CANADA reported BETASERON problem on June 26, 2007. Female patient, 58 years of age, was diagnosed with secondary progressive multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, joint range of motion decreased, mobility decreased, muscular weakness, . BETASERON dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Betaseron Side Effects Report #5377582-9
BETASERON problem was reported by a Consumer or non-health professional from CANADA on June 26, 2007. Female patient, 58 years of age, was diagnosed with secondary progressive multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, joint range of motion decreased, mobility decreased, muscular weakness, . BETASERON dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5667982-1
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 11, 2008. Female patient, weighting 183.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: bacteria urine, joint range of motion decreased, . HUMIRA dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5668304-2
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 19, 2008. Female patient, weighting 120.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: cough, influenza, joint range of motion decreased, joint stiffness, neck pain, . HUMIRA dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5668325-X
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Feb 19, 2008. Male patient, weighting 201.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: impaired work ability, joint range of motion decreased, rheumatoid arthritis, . HUMIRA dosage: unknown. During the same period patient was treated with HYDROXYCHLOROQUINE PHOSPHATE, SULFASALAZINE, OXAPROZIN. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Avonex Side Effects Report #5681121-2
AVONEX problem was reported by a Consumer or non-health professional from on Mar 13, 2008. Male patient, 52 years of age, weighting 165.3 lb, was diagnosed with multiple sclerosis and was treated with AVONEX. After drug was administered, patient experienced the following problems/side effects: arthralgia, influenza like illness, joint range of motion decreased, knee arthroplasty, multiple sclerosis relapse, postoperative thrombosis, . AVONEX dosage: unknown. During the same period patient was treated with BACLOFEN, IBUPROFEN. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Mirena Side Effects Report #5625610-5
Consumer or non-health professional from UNITED STATES reported MIRENA problem on Jan 18, 2008. Female patient, 28 years of age, weighting 145.5 lb, was diagnosed with contraception and was treated with MIRENA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, back pain, joint range of motion decreased, libido decreased, metrorrhagia, . MIRENA dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Fosamax Side Effects Report #5627607-8
FOSAMAX problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 14, 2008. Female patient, 58 years of age, weighting 117.0 lb, was diagnosed with osteopenia and was treated with FOSAMAX. After drug was administered, patient experienced the following problems/side effects: arthralgia, bone pain, joint range of motion decreased, musculoskeletal pain, myalgia, neck pain, pain in extremity, . FOSAMAX dosage: unknown. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Gadolinium Side Effects Report #5633063-6
Health Professional from UNITED STATES reported GADOLINIUM CONTRAST MEDIA problem on Feb 06, 2008. Male patient, 48 years of age, was diagnosed with mental status changes and was treated with GADOLINIUM CONTRAST MEDIA. After drug was administered, patient experienced the following problems/side effects: abdominal abscess, hypotension, joint range of motion decreased, nephrogenic systemic fibrosis, oedema peripheral, pain in extremity, rash erythematous, rash papular, skin hypertrophy, . GADOLINIUM CONTRAST MEDIA dosage: unknown. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5645732-2
HUMIRA problem was reported by a Physician from UNITED STATES on Feb 29, 2008. Male patient, weighting 182.2 lb, was diagnosed with rheumatoid arthritis, vitamin supplementation, pain and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthropathy, c-reactive protein increased, joint range of motion decreased, mobility decreased, pain, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, FOLIC ACID, PROPACET. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5571896-5
Health Professional from UNITED KINGDOM reported HUMIRA problem on Dec 11, 2007. Female patient, weighting 154.3 lb, was diagnosed with arthritis bacterial, analgesia, hypertension, psoriatic arthropathy and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthritis bacterial, erythema, joint range of motion decreased, . HUMIRA dosage: unknown. During the same period patient was treated with ACETAMINOPHEN W, ATENOLOL, METHOTREXATE, FOLIC ACID. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Enbrel Side Effects Report #5519242-7
ENBREL problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 07, 2007. Female patient was diagnosed with rheumatoid arthritis, juvenile arthritis and was treated with ENBREL. After drug was administered, patient experienced the following problems/side effects: device failure, hypoaesthesia, joint range of motion decreased, rheumatoid arthritis, spondylitis, . ENBREL dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Betaseron Side Effects Report #5449257-9
Consumer or non-health professional from CANADA reported BETASERON problem on Aug 30, 2007. Female patient, 58 years of age, was diagnosed with secondary progressive multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: gait disturbance, hypoaesthesia, joint range of motion decreased, mobility decreased, muscular weakness, musculoskeletal stiffness, sensation of heaviness, . BETASERON dosage: unknown. During the same period patient was treated with ADVIL LIQUI. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Humira Side Effects Report #5453298-5
HUMIRA problem was reported by a Health Professional from FRANCE on Sept 10, 2007. Male patient was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: dermatitis, erythema, joint range of motion decreased, lichenoid keratosis, pain, rash maculo-papular, skin lesion, . HUMIRA dosage: unknown. During the same period patient was treated with PREDNISONE, METHOTREXATE, FOLIC ACID, ALENDRONATE MONOSODIC, OMEPRAZOLE, CALCIUM D, CLONAZEPAM. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Accutane Side Effects Report #5474110-4
Physician from UNITED STATES reported ACCUTANE problem on Sept 27, 2007. Male patient, weighting 125.0 lb, was diagnosed with acne and was treated with ACCUTANE. After drug was administered, patient experienced the following problems/side effects: anxiety, arthralgia, joint range of motion decreased, muscle rupture, musculoskeletal pain, osteoporosis, . ACCUTANE dosage: 60 MG DAILY PO. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Betaseron Side Effects Report #5420106-8
BETASERON problem was reported by a Consumer or non-health professional from CANADA on Aug 15, 2007. Female patient, 58 years of age, was diagnosed with secondary progressive multiple sclerosis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: gait disturbance, hypoaesthesia, joint range of motion decreased, mobility decreased, muscular weakness, musculoskeletal stiffness, sensation of heaviness, . BETASERON dosage: unknown. During the same period patient was treated with ADVIL LIQUI. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Betaseron Side Effects Report #5379285-3
Consumer or non-health professional from CANADA reported BETASERON problem on June 20, 2007. Male patient, 45 years of age, weighting 187.4 lb, was diagnosed with relapsing-remitting multiple sclerosis, insomnia, prophylaxis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: dysphagia, hypoaesthesia, joint range of motion decreased, muscle spasms, oedema peripheral, pain, pharyngeal oedema, pneumonia, pollakiuria, . BETASERON dosage: unknown. During the same period patient was treated with IMOVANE, PAXIL, PROGRAF, ZANAFLEX. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Actonel Side Effects Report #5391259-5
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 68 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, gait disturbance, joint range of motion decreased, osteoarthritis, . ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with DYNACIRC CR, SPIRONOLACTONE, SYNTHROID, CALCIUM, GLUCOSAMINE, CRANBERRY. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Betaseron Side Effects Report #5379285-3
Consumer or non-health professional from CANADA reported BETASERON problem on June 20, 2007. Male patient, 45 years of age, weighting 187.4 lb, was diagnosed with relapsing-remitting multiple sclerosis, insomnia, prophylaxis and was treated with BETASERON. After drug was administered, patient experienced the following problems/side effects: dysphagia, hypoaesthesia, joint range of motion decreased, muscle spasms, oedema peripheral, pain, pharyngeal oedema, pneumonia, pollakiuria, . BETASERON dosage: unknown. During the same period patient was treated with IMOVANE, PAXIL, PROGRAF, ZANAFLEX. Patient was hospitalized. Patient recovered.
JOINT RANGE OF MOTION DECREASED : Actonel Side Effects Report #5391259-5
ACTONEL problem was reported by a Consumer or non-health professional from UNITED STATES on July 05, 2007. Female patient, 68 years of age, was treated with ACTONEL. After drug was administered, patient experienced the following problems/side effects: arthralgia, gait disturbance, joint range of motion decreased, osteoarthritis, . ACTONEL dosage: 35 MG ONCE WEEKLY, ORAL. During the same period patient was treated with DYNACIRC CR, SPIRONOLACTONE, SYNTHROID, CALCIUM, GLUCOSAMINE, CRANBERRY. Patient recovered.