Mobic Side Effects
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Mobic Safety Reports reported to FDA
Total Mobic reports: 126.Mobic FDA safety alerts: No.
Reported deaths: 21 Reported hospitalizations: 81.
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Reported Mobic Side Effects: renal failure acute, pain in extremity, haemorrhage subcutaneous, chest pain, gastric ulcer perforation, diarrhoea, vomiting, nausea, blood creatine phosphokinase increased, arthralgia, sick sinus syndrome.
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< Previous Showing 101-126 of 126
Mobic Side Effects Report #5399585-0Physician from AUSTRALIA reported MOBIC problem on July 25, 2007. Male patient, weighting 180.8 lb, was diagnosed with osteoarthritis, prophylaxis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: gastrointestinal haemorrhage. MOBIC dosage: unknown. During the same period patient was treated with CARTIA XT, AUGMENTINTE. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5401844-X
MOBIC problem was reported by a Physician from JAPAN on July 26, 2007. Female patient, 60 years of age, was diagnosed with musculoskeletal pain, tachycardia and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: agranulocytosis. MOBIC dosage: unknown. During the same period patient was treated with BEPRICOR, METHOTREXATE. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5405391-0
Physician from JAPAN reported MOBIC problem on July 27, 2007. Female patient, weighting 123.5 lb, was diagnosed with musculoskeletal pain, atrial flutter, pleurisy, cellulitis, iron deficiency anaemia and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: granulocytopenia, renal impairment. MOBIC dosage: unknown. During the same period patient was treated with BEPRICOR, RHEUMATREX, CIPROFLOXACIN, PREDNISOLONE, FERROMIA, UNASYN. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5405396-X
MOBIC problem was reported by a Physician from on July 31, 2007. Female patient, 70 years of age, weighting 251.3 lb, was diagnosed with obesity, sarcoidosis, hypothyroidism and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, cardiac flutter, diarrhoea, epistaxis, fatigue, heart rate increased, tremor. MOBIC dosage: unknown. During the same period patient was treated with ACOMPLIA, ATROVENT, FELDENE, LEVOTHYROXINE, METFORMIN, MIZOLASTINE, MEMETASONE, NEDOCROMIL. Patient recovered.
Mobic Side Effects Report #5407585-7
Health Professional from UNITED STATES reported MOBIC problem on July 31, 2007. Female patient, 49 years of age, was diagnosed with arthralgia and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: bladder prolapse, haematocrit decreased, haemorrhage, post procedural haemorrhage. MOBIC dosage: unknown. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5407592-4
MOBIC problem was reported by a Physician from JAPAN on July 31, 2007. Female patient, 78 years of age, was diagnosed with polymyalgia rheumatica, hyperlipidaemia, osteoporosis, diabetes mellitus and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, gait disturbance, myalgia. MOBIC dosage: unknown. During the same period patient was treated with SIMVASTATIN, ACTONEL, GLIMICRON, KINEDAK, METHYCOBAL, ANPLAG, DEPAS. Patient recovered.
Mobic Side Effects Report #5417190-4
Physician from JAPAN reported MOBIC problem on Aug 09, 2007. Female patient, weighting 92.59 lb, was diagnosed with polymyalgia rheumatica, hyperlipidaemia, osteoporosis, type 2 diabetes mellitus, insomnia, constipation and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, blood creatine phosphokinase increased, gait disturbance, muscular weakness, musculoskeletal stiffness, pain, pain in extremity. MOBIC dosage: unknown. During the same period patient was treated with SIMVASTATIN, ACTONEL, GLIMICRON, KINEDAK, METHYCOBAL, ANPLAG, DEPAS, PURSENNID. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5417197-7
MOBIC problem was reported by a Physician from JAPAN on Aug 09, 2007. Female patient, 37 years of age, was diagnosed with rheumatoid arthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: eosinophil count increased, face oedema. MOBIC dosage: unknown. During the same period patient was treated with RIMATIL. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5419204-4
Physician from reported MOBIC problem on Aug 14, 2007. Female patient, 70 years of age, was diagnosed with obesity, sarcoidosis, hypothyroidism and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, fatigue, heart rate increased, tremor. MOBIC dosage: unknown. During the same period patient was treated with ACOMPLIA, ATROVENT, FELDENE, LEVOTHYROXINE, METFORMIN, MIZOLASTINE, MEMETASONE, NEDOCROMIL. Patient recovered.
Mobic Side Effects Report #5419206-8
MOBIC problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Male patient, 72 years of age, was diagnosed with osteoarthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: axillary pain, back pain, chest pain, coronary artery disease, dizziness, dizziness exertional, electrocardiogram st segment depression, hyperhidrosis, hypoaesthesia. MOBIC dosage: unknown. During the same period patient was treated with GLUCOSAMINE AND CHONDROITIN, ALKA SELTZER, CLARITIN, BISACODYL, TYLENOL, IMODIUM. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5420170-6
Consumer or non-health professional from UNITED STATES reported MOBIC problem on Aug 15, 2007. Female patient, 49 years of age, was diagnosed with arthralgia and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: bladder prolapse, haematocrit decreased, haemorrhage, post procedural haemorrhage. MOBIC dosage: unknown. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5422274-0
MOBIC problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, 52 years of age, weighting 200.0 lb, was diagnosed with osteoarthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: muscle spasms. MOBIC dosage: 75 MG 2 TIMES A DAY PO. Patient recovered.
Mobic Side Effects Report #5424278-0
Physician from JAPAN reported MOBIC problem on Aug 09, 2007. Female patient, weighting 93.70 lb, was diagnosed with polymyalgia rheumatica, hyperlipidaemia, osteoporosis, type 2 diabetes mellitus, insomnia, constipation and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, muscular weakness, pain. MOBIC dosage: unknown. During the same period patient was treated with SIMVASTATIN, ACTONEL, GLIMICRON, KINEDAK, METHYCOBAL, ANPLAG, DEPAS, PURSENNID. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5424292-5
MOBIC problem was reported by a Physician from COLOMBIA on Aug 21, 2007. Female patient, 60 years of age, was diagnosed with arthralgia and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: infarction. MOBIC dosage: unknown. Patient died.
Mobic Side Effects Report #5426807-X
Physician from COLOMBIA reported MOBIC problem on Aug 24, 2007. Female patient, 60 years of age, was diagnosed with arthralgia and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: myocardial infarction. MOBIC dosage: unknown. Patient died.
Mobic Side Effects Report #5429928-0
MOBIC problem was reported by a Physician from JAPAN on Aug 24, 2007. Female patient, weighting 113.8 lb, was diagnosed with rheumatoid arthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: eosinophil count increased, face oedema. MOBIC dosage: unknown. During the same period patient was treated with RIMATIL. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5440624-6
Physician from reported MOBIC problem on Aug 28, 2007. Male patient, 45 years of age, weighting 176.4 lb, was diagnosed with osteoarthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: myocardial infarction. MOBIC dosage: unknown. During the same period patient was treated with CELEBREX, NAPROXEN, SYNVISC, CAPSAICIN. Patient died on 11/27/2004.
Mobic Side Effects Report #5440627-1
MOBIC problem was reported by a Physician from on Aug 28, 2007. Male patient, 45 years of age, weighting 176.4 lb, was diagnosed with osteoarthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: myocardial infarction. MOBIC dosage: unknown. During the same period patient was treated with CELEBREX, NAPROXEN, SYNVISC, CAPSAICIN. Patient died on 11/27/2004.
Mobic Side Effects Report #5441598-4
Consumer or non-health professional from UNITED STATES reported MOBIC problem on Aug 30, 2007. Male patient, weighting 230.0 lb, was diagnosed with arthropathy, inflammation and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: urinary retention, urinary tract infection. MOBIC dosage: 7.5 MG 2 TIMES/DAY MOUTH. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5442794-2
MOBIC problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, 52 years of age, was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: gastrooesophageal reflux disease. MOBIC dosage: unknown. Patient recovered.
Mobic Side Effects Report #5443916-X
Physician from reported MOBIC problem on Aug 31, 2007. Female patient, 57 years of age, was diagnosed with cancer pain, nausea, vaginal haemorrhage and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, haemorrhage, renal impairment. MOBIC dosage: unknown. During the same period patient was treated with DOMPERIDONE, OMEPRAZOLE, OXYCONTIN, TRANEXAMIC ACID. Patient recovered.
Mobic Side Effects Report #5443919-5
MOBIC problem was reported by a Physician from FRANCE on Aug 30, 2007. Female patient, 76 years of age, was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: bone marrow failure, stevens-johnson syndrome. MOBIC dosage: unknown. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5443920-1
Physician from reported MOBIC problem on Aug 29, 2007. Female patient, 63 years of age, was diagnosed with osteoarthritis and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: abdominal pain, dyspnoea, malaise, oral pain, pruritus, stomatitis. MOBIC dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
Mobic Side Effects Report #5445514-0
MOBIC problem was reported by a Physician from JAPAN on Aug 30, 2007. Female patient, weighting 93.70 lb, was diagnosed with polymyalgia rheumatica, hyperlipidaemia, osteoporosis, type 2 diabetes mellitus, insomnia, constipation and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, eosinophil count increased, muscular weakness, pain. MOBIC dosage: unknown. During the same period patient was treated with SIMVASTATIN, ACTONEL, GLIMICRON, KINEDAK, METHYCOBAL, ANPLAG, DEPAS, PURSENNID. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5451599-8
Physician from JAPAN reported MOBIC problem on Aug 30, 2007. Female patient, weighting 93.70 lb, was diagnosed with polymyalgia rheumatica, hyperlipidaemia, osteoporosis, type 2 diabetes mellitus, insomnia, constipation and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: blood creatine phosphokinase increased, eosinophil count increased, muscular weakness, pain. MOBIC dosage: unknown. During the same period patient was treated with SIMVASTATIN, ACTONEL, GLIMICRON, KINEDAK, METHYCOBAL, ANPLAG, DEPAS, PURSENNID. Patient was hospitalized. Patient recovered.
Mobic Side Effects Report #5453009-3
MOBIC problem was reported by a Physician from on Sept 13, 2007. Female patient, 82 years of age, was diagnosed with pain and was treated with MOBIC. After drug was administered, patient experienced the following problems/side effects: arteriosclerosis, aspiration, coronary artery disease, intestinal ischaemia, pericarditis. MOBIC dosage: unknown. During the same period patient was treated with DIGOXIN, FOLIC ACID, OMEPRAZOLE, VITAMIN D. Patient died on 01/01/2007.
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Drug Information: Meloxicam
URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a601242.html
(mel ox' i cam)IMPORTANT WARNING:
| People who take nonsteroidal anti-inflammatory medications (NSAIDs) (other than aspirin) such as meloxicam may have a higher risk of having a heart attack or a stroke than people who do not take these medications. These events may happen without warning and may cause death. This risk may be higher for people who take NSAIDs for a long time. Tell your doctor if you or anyone in your family has or has ever had heart disease, a heart attack, or a stroke, if you smoke, and if you have or have ever had high cholesterol, high blood pressure, or diabetes. Get emergency medical help right away if you experience any of the following symptoms: chest pain, shortness of breath, weakness in one part or side of the body, or slurred speech.If you will be undergoing a coronary artery bypass graft (CABG; a type of heart surgery), you should not take meloxicam right before or right after the surgery.NSAIDs such as meloxicam may cause ulcers, bleeding, or holes in the stomach or intestine. These problems may develop at any time during treatment, may happen without warning symptoms, and may cause death. The risk may be higher for people who take NSAIDs for a long time, are older in age, have poor health, or drink large amounts of alcohol while you are taking meloxicam. Tell your doctor if you take any of the following medications: anticoagulants ('blood thinners') such as warfarin (Coumadin); aspirin; other NSAIDs such as ibuprofen (Advil, Motrin) or naproxen (Aleve, Naprosyn); or oral steroids such as dexamethasone (Decadron, Dexone), methylprednisolone (Medrol), and prednisone (Deltasone). Also tell your doctor if you have or have ever had ulcers or bleeding in your stomach or intestines, or other bleeding disorders. If you experience any of the following symptoms, stop taking meloxicam and call your doctor: stomach pain, heartburn, vomiting a substance that is bloody or looks like coffee grounds, blood in the stool, or black and tarry stools.Keep all appointments with your doctor and the laboratory. Your doctor will monitor your symptoms carefully and will probably order certain tests to check your body's response to meloxicam. Be sure to tell your doctor how you are feeling so that your doctor can prescribe the right amount of medication to treat your condition with the lowest risk of serious side effects.Your doctor or pharmacist will give you the manufacturer's patient information sheet (Medication Guide) when you begin treatment with meloxicam and each time you refill your prescription. Read the information carefully and ask your doctor or pharmacist if you have any questions. You can also visit the Food and Drug Administration (FDA) website (http://www.fda.gov/cder) or the manufacturer's website to obtain the Medication Guide. |
Why is this medication prescribed?
Meloxicam is used to relieve pain, tenderness, swelling, and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints) and rheumatoid arthritis (arthritis caused by swelling of the lining of the joints). Meloxicam is also used to relieve the pain, tenderness,swelling, and stiffness caused by juvenile rheumatoid arthritis (a type of arthritis that affects children) in children 2 years of age and older. Meloxicam is in a class of medications called nonsteroidal anti-inflammatory medications (NSAIDs). It works by stopping the body's production of a substance that causes pain, fever, and inflammation.
How should this medicine be used?
Meloxicam comes as a tablet and suspension (liquid) to take by mouth. It is usually taken once a day with or without food. Take meloxicam at the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take meloxicam exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.
Shake the suspension well before each use to mix the medication evenly.
Other uses for this medicine
Meloxicam is also used sometimes to treat ankylosing spondylitis (arthritis that mainly affects the spine). Talk to your doctor about the possible risks of using this medication for your condition.
This medication may be prescribed for other uses; ask your doctor or pharmacist for more information.
What special precautions should I follow?
Before taking meloxicam,
- tell your doctor and pharmacist if you are allergic to meloxicam, aspirin or other NSAIDs such as ibuprofen (Advil, Motrin) and naproxen (Aleve, Naprosyn), or any other medications.
- tell your doctor and pharmacist what prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Be sure to mention the medications listed in the IMPORTANT WARNING section and any of the following: angiotensin-converting enzyme (ACE) inhibitors such as benazepril (Lotensin), captopril (Capoten), enalapril (Vasotec), fosinopril (Monopril), lisinopril (Prinivil, Zestril), and quinapril (Accupril); cholestyramine (Questran); diuretics ('water pills'); lithium (Eskalith, Lithobid, others); and methotrexate (Rheumatrex). Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
- tell your doctor if you have or have ever had asthma, especially if you have frequent stuffed or runny nose or nasal polyps (swelling of the lining of the nose); swelling of the hands, feet, ankles, or lower legs; or kidney or liver disease.
- tell your doctor if you are pregnant, especially if you are in the last few months of your pregnancy, you plan to become pregnant, or you are breast-feeding. If you become pregnant while taking meloxicam, call your doctor.
- if you are having surgery, including dental surgery, tell the doctor or dentist that you are taking meloxicam.
What should I do if I forget a dose?
Take the missed dose as soon as you remember it. However, if it is almost time for the next dose, skip the missed dose and continue your regular dosing schedule. Do not take a double dose to make up for a missed one.
What side effects can this medication cause?
Meloxicam may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:
- diarrhea
- constipation
- gas
- sore throat
- cough
- runny nose
Some side effects can be serious. If you experience any of the following symptoms, call your doctor immediately. Do not take any more meloxicam until you speak to your doctor:
- fever
- blisters
- rash
- hives
- itching
- swelling of the eyes, face, tongue, lips,throat, arms, hands, feet, ankles, or lower legs
- difficulty breathing or swallowing
- hoarseness
- pale skin
- fast heartbeat
- unexplained weight gain
- upset stomach
- excessive tiredness
- lack of energy
- yellowing of the skin or eyes
- pain in the right upper part of the stomach
- flu-like symptoms
- cloudy, discolored, or bloody urine
- back pain
- difficult or painful urination
Meloxicam may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.
If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].
What storage conditions are needed for this medicine?
Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it at room temperature and away from excess heat and moisture (not in the bathroom). Throw away any medication that is outdated or no longer needed. Talk to your pharmacist about the proper disposal of your medication.
In case of emergency/overdose
In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.
Symptoms of overdose may include:
- lack of energy
- drowsiness
- upset stomach
- vomiting
- stomach pain
- bloody, black, or tarry stools
- vomiting a substance that is bloody or looks like coffee grounds
- difficulty breathing
- seizures
- coma
What other information should I know?
Do not let anyone else take your medication. Ask your pharmacist any questions you have about refilling your prescription.
It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.
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