JOINT RANGE OF MOTION DECREASED side effect
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Drugs associated with JOINT RANGE OF MOTION DECREASED
ACCUTANE ACTONEL ARIMIDEX AVANDIA AVONEX BETASERON BONIVA BOTOX CEFTRIAXONE CIPROFLOXACIN CLARAVIS CLONAZEPAM COMPAZINE CRESTOR FOSAMAX GADOLINIUM HUMIRA INFERGEN JANUMET LEVAQUIN LIPITOR LYRICA MAGNEVIST MIRENA MOBIC NOVANTRONE NUTROPIN OMNISCAN PACERONE PLAVIX PRIALT PULMICORT RECLAST REMICADE RENAGEL RIBAVIRIN ROCEPHIN SENSORCAINE SPIRIVA VYTORIN ZOCOR ZOMETABotox 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.
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.
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.
Ciprofloxacin Side Effects Report #5549355-5
CIPROFLOXACIN problem was reported by a Health Professional from SPAIN 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.
Avonex Side Effects Report #5567876-6
Consumer or non-health professional from UNITED STATES reported AVONEX problem 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.
Avandia Side Effects Report #5452883-4
AVANDIA problem was reported by a Consumer or non-health professional from UNITED STATES 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.
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.
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.
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.
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.
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.
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.
Humira Side Effects Report #5768557-6
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 07, 2008. Female patient, weighting 180.2 lb, was diagnosed with rheumatoid arthritis, hyperlipidaemia, hiatus hernia, hypertension and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, pain, wound, . HUMIRA dosage: unknown. During the same period patient was treated with INEGY, ESOMEPRAZOLE MAGNESIUM, METOPROLOL SUCCINATE. Patient recovered.
Botox Side Effects Report #5726983-5
BOTOX problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 29, 2008. Female patient, child 5 years of age, 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, muscle tightness, . BOTOX dosage: unknown. Patient recovered.
Boniva Side Effects Report #5743720-9
Consumer or non-health professional from UNITED STATES reported BONIVA problem on May 09, 2008. Female patient, 81 years of age, was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, nausea, weight decreased, . BONIVA dosage: unknown. Patient recovered.
Ribavirin Side Effects Report #5754856-0
RIBAVIRIN problem was reported by a Health Professional from UNITED STATES on May 16, 2008. Male patient, 54 years of age, was diagnosed with hepatitis c virus and was treated with RIBAVIRIN. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, movement disorder, musculoskeletal pain, . RIBAVIRIN dosage: (1200 MG [200 MG X 6] ORAL). During the same period patient was treated with INFERGEN. Patient recovered.
Infergen Side Effects Report #5754896-1
Health Professional from UNITED STATES reported INFERGEN problem on May 16, 2008. Male patient, 54 years of age, was diagnosed with hepatitis c virus and was treated with INFERGEN. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, musculoskeletal pain, . INFERGEN dosage: unknown. During the same period patient was treated with RIBAVIRIN. Patient recovered.
Ceftriaxone Side Effects Report #5330965-5
CEFTRIAXONE problem was reported by a Pharmacist from FRANCE on May 11, 2007. Male patient, 75 years of age, was diagnosed with respiratory disorder and was treated with CEFTRIAXONE. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, . CEFTRIAXONE dosage: unknown. Patient recovered.
Avonex Side Effects Report #5314563-5
Consumer or non-health professional from UNITED STATES reported AVONEX problem on Apr 10, 2007. Female patient, 57 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, . AVONEX dosage: unknown. Patient was hospitalized. Patient recovered.
Levaquin Side Effects Report #5258760-6
LEVAQUIN problem was reported by a Consumer or non-health professional from UNITED STATES on Jan 09, 2006. Female patient, 64 years of age, weighting 153.0 lb, was diagnosed with ulcer and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, musculoskeletal pain, . LEVAQUIN dosage: 500 MG, 1 IN 1 DAY, ORAL. Patient recovered.
Levaquin Side Effects Report #5262269-3
Consumer or non-health professional from UNITED STATES reported LEVAQUIN problem on Mar 08, 2007. Female patient, 34 years of age, weighting 130.0 lb, was diagnosed with bronchitis and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, rash, . LEVAQUIN dosage: unknown. Patient was hospitalized. Patient recovered.
Rocephin Side Effects Report #5263611-X
ROCEPHIN problem was reported by a Pharmacist from FRANCE on Mar 01, 2007. Male patient, 75 years of age, was diagnosed with respiratory disorder and was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, . ROCEPHIN dosage: unknown. Patient recovered.
Lipitor Side Effects Report #5267829-1
Consumer or non-health professional from NETHERLANDS reported LIPITOR problem on Mar 07, 2007. Male patient, weighting 198.4 lb, was diagnosed with hypercholesterolaemia and was treated with LIPITOR. After drug was administered, patient experienced the following problems/side effects: joint range of motion decreased, myalgia, tongue disorder, . LIPITOR dosage: unknown. During the same period patient was treated with OMEPRAZOLE, METFORMIN, ACETYLSALICYLIC ACID SRT, INSULATARD. Patient recovered.
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.
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.
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.
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.
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.
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.
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.
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.
Zometa Side Effects Report #5424664-9
ZOMETA problem was reported by a Consumer or non-health professional from GERMANY 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.
Pacerone Side Effects Report #5424765-5
Consumer or non-health professional from UNITED STATES reported PACERONE problem 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.
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.
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.
Sensorcaine Side Effects Report #5764155-9
SENSORCAINE problem was reported by a Physician from UNITED STATES on May 22, 2008. Male patient, 18 years of age, was diagnosed with musculoskeletal pain, surgery and was treated with SENSORCAINE. After drug was administered, patient experienced the following problems/side effects: chondrolysis, joint range of motion decreased, movement disorder, musculoskeletal pain, . SENSORCAINE dosage: unknown. During the same period patient was treated with XYLOCAINE, MITEK THERMAL PROBE, DONJOY PAIN PUMP, ANTIBIOTICS. Patient was hospitalized and became disabled. Patient recovered.
Humira Side Effects Report #5768671-5
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on Mar 11, 2008. Female patient, weighting 206.2 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: injection site laceration, joint range of motion decreased, swelling, . HUMIRA dosage: unknown. During the same period patient was treated with MELOXICAM. Patient recovered.
Humira Side Effects Report #5769602-4
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 01, 2008. Female patient, weighting 130.1 lb, was diagnosed with rheumatoid arthritis, autoimmune thyroiditis, folate deficiency, prophylaxis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, pain, rheumatoid arthritis, . HUMIRA dosage: unknown. During the same period patient was treated with LEVOTHYROXINE, METHOTREXATE, PREDNISONE, FOLIC ACID, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE MAGNESIUM. Patient recovered.
Humira Side Effects Report #5770547-4
Consumer or non-health professional from UNITED STATES reported HUMIRA problem on May 06, 2008. Male patient, weighting 180.2 lb, was diagnosed with rheumatoid arthritis, hypertension, cardiac disorder, depression, diabetes mellitus, pain, headache and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: influenza, joint range of motion decreased, pain, . HUMIRA dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, DIGOXIN, VENLAFAXINE HYDROCHLORIDE, JENUVIA, MONTELUKAST, ASPIRIN, ACETAMINOPHEN, DICLOFENAC. Patient recovered.
Humira Side Effects Report #5770981-2
HUMIRA problem was reported by a Consumer or non-health professional from UNITED STATES on May 22, 2008. Female patient, weighting 160.1 lb, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: dysstasia, joint range of motion decreased, pain in extremity, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE, CANDESARTAN CILEXETIL, FOLIC ACID, ATORVASTATIN CALCIUM, ASPIRIN. Patient recovered.
Novantrone Side Effects Report #5778960-6
Physician from UNITED STATES reported NOVANTRONE problem on Dec 04, 2007. Female patient, 46 years of age, weighting 190.0 lb, was diagnosed with multiple sclerosis and was treated with NOVANTRONE. After drug was administered, patient experienced the following problems/side effects: extravasation, joint range of motion decreased, oedema peripheral, pain, sensory loss, skin discolouration, . NOVANTRONE dosage: 21.6 MG, 1 IN 3 MONTHS, INTRAVENOUS. Patient recovered.
Humira Side Effects Report #5782572-8
HUMIRA problem was reported by a Physician from ARGENTINA on June 08, 2008. Female patient, 60 years of age, was diagnosed with rheumatoid arthritis and was treated with HUMIRA. After drug was administered, patient experienced the following problems/side effects: gait disturbance, joint range of motion decreased, leukocytoclastic vasculitis, nodule on extremity, rheumatoid nodule, . HUMIRA dosage: unknown. During the same period patient was treated with METHOTREXATE. Patient was hospitalized. Patient recovered.
Boniva Side Effects Report #5794897-0
Consumer or non-health professional from UNITED STATES reported BONIVA problem on June 27, 2008. Female patient, weighting 140.0 lb, was diagnosed with osteoporosis and was treated with BONIVA. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, joint swelling, musculoskeletal pain, musculoskeletal stiffness, myalgia, neck pain, nerve compression, . BONIVA dosage: unknown. During the same period patient was treated with FOSOMAX. Patient recovered.
Levaquin Side Effects Report #5742741-X
LEVAQUIN problem was reported by a Physician from UNITED STATES on May 15, 2008. Female patient, weighting 218.0 lb, was diagnosed with skin irritation and was treated with LEVAQUIN. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, lip ulceration, oedema peripheral, pain in extremity, tendon pain, urticaria, . LEVAQUIN dosage: 750 MG PO QD X 5D (ONLY TOOK 3 DOSES). Patient recovered.
Claravis Side Effects Report #5758994-8
Consumer or non-health professional from TURKEY reported CLARAVIS problem on May 15, 2008. Female patient, 25 years of age, was diagnosed with acne and was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: back pain, joint range of motion decreased, musculoskeletal stiffness, sacroiliitis, . CLARAVIS dosage: unknown. Patient was hospitalized. Patient recovered.
Claravis Side Effects Report #5758996-1
CLARAVIS problem was reported by a Consumer or non-health professional from TURKEY on May 15, 2008. Male patient, 24 years of age, was diagnosed with acne and was treated with CLARAVIS. After drug was administered, patient experienced the following problems/side effects: back pain, joint range of motion decreased, musculoskeletal stiffness, sacroiliitis, . CLARAVIS dosage: unknown. Patient was hospitalized. Patient recovered.
Lyrica Side Effects Report #5693913-4
Consumer or non-health professional from UNITED STATES reported LYRICA problem on Mar 25, 2008. Female patient, weighting 123.9 lb, was diagnosed with pain and was treated with LYRICA. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, joint swelling, . LYRICA dosage: unknown. During the same period patient was treated with ACETAMINOPHEN AND OXYCODONE, RITALIN, CYMBALTA, MAGNESIUM. Patient recovered.
Compazine Side Effects Report #5694416-3
COMPAZINE problem was reported by a Health Professional from UNITED STATES on Apr 03, 2008. Female patient was diagnosed with cyclic vomiting syndrome and was treated with COMPAZINE. After drug was administered, patient experienced the following problems/side effects: dyskinesia, joint range of motion decreased, . COMPAZINE dosage: 5 MG EVERY 6 HOURS PRN IV. Patient recovered.
Vytorin Side Effects Report #5697804-4
Consumer or non-health professional from UNITED STATES reported VYTORIN problem on Apr 01, 2008. Male patient, 56 years of age, was treated with VYTORIN. After drug was administered, patient experienced the following problems/side effects: asthenia, joint range of motion decreased, musculoskeletal stiffness, myalgia, . VYTORIN dosage: unknown. During the same period patient was treated with PLAVIX, FUROSEMIDE, GLUCOPHAGE, OMEGA, COREG, ASPIRIN. Patient recovered.
Janumet Side Effects Report #5716121-7
JANUMET problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 23, 2008. Male patient, 49 years of age, weighting 140.0 lb, was diagnosed with blood glucose abnormal and was treated with JANUMET. After drug was administered, patient experienced the following problems/side effects: activities of daily living impaired, joint range of motion decreased, musculoskeletal pain, . JANUMET dosage: unknown. Patient recovered.
Pulmicort Side Effects Report #5720966-7
Health Professional from UNITED STATES reported PULMICORT problem on Apr 25, 2008. Female patient, 48 years of age, weighting 155.0 lb, was diagnosed with asthma and was treated with PULMICORT. After drug was administered, patient experienced the following problems/side effects: arthralgia, joint range of motion decreased, . PULMICORT dosage: unknown. Patient recovered.