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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Mobic (Meloxicam). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (114)
Cases resulting in a serious event (103)
Cases resulting in death (13)
Cases resulting in life threatening events (13)
Cases resulting in hospitalization (71)
Cases resulting in disability (5)
Cases resulting in other serious reactions (22)
Below is a sample of reports where side effects / adverse reactions may be related to Mobic (Meloxicam). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 62 year old male receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from United States on 2007-10-30
Patient: 62 year old male
Adverse reactions / side effects: Cataract, Orthostatic Hypotension, Headache, Posture Abnormal, Somnolence, Vision Blurred, Dizziness, Transient Ischaemic Attack, Asthenia
Suspect drug(s):
Mobic
Indication: Osteoarthritis
Start date: 2007-05-31
Study Drug
Indication: Osteoarthritis
Other drugs received by patient: Aspirin
Adverse event in female receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-30
Patient: female
Adverse reactions / side effects: Fatigue, Palpitations, Arthralgia, Gastroenteritis Viral
Suspect drug(s):
Mobic (Meloxicam)
Other drugs received by patient: Theophylline; Hyzaar; Synthroid; Allegra D 24 Hour; Allopurinol; Alupent; Advair Diskus 100 / 50
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Japan on 2007-10-26
Patient: female, weighing 67.0 kg (147.4 pounds)
Adverse reactions / side effects: Tuberculosis, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Remicade
Dosage: 9 infusions on unknown dates
Indication: Rheumatoid Arthritis
Mobic
Administration route: Oral
Indication: Rheumatoid Arthritis
Bredinin
Administration route: Oral
Indication: Rheumatoid Arthritis
Rimatil
Administration route: Oral
Indication: Rheumatoid Arthritis
Actonel
Administration route: Oral
Indication: Osteoporosis
Lansoprazole
Administration route: Oral
Indication: Reflux Oesophagitis
Cytotec
Dosage: 600rg
Administration route: Oral
Indication: Gastritis
Rheumatrex
Administration route: Oral
Indication: Rheumatoid Arthritis
Other drugs received by patient: Isoniazid
Adverse event in female receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-24
Patient: female
Adverse reactions / side effects: Rash Pruritic
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Arthritis
Start date: 2007-10-01
End date: 2007-10-01
Mobic
Indication: Synovial Cyst
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-23
Patient: female
Adverse reactions / side effects: Oedema Peripheral, Ankle Fracture, Fall
Adverse event resulted in: hospitalization
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in male receiving Mobic (Meloxicam)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-23
Patient: male, weighing 100.0 kg (220.0 pounds)
Adverse reactions / side effects: Erythrosis, Cholestasis, Hepatic Failure, Upper Respiratory Tract Infection, Sleep Disorder, Gallbladder Disorder, Thrombocytopenia, Hypergammaglobulinaemia, Acute Prerenal Failure, Hepatitis Fulminant
Adverse event resulted in: hospitalization
Suspect drug(s):
Effexor XR
Dosage: unknown
Administration route: Oral
Indication: Depression
Start date: 2007-03-01
End date: 2007-09-01
Amlor
Administration route: Oral
End date: 2007-09-01
Mobic
Dosage: unknown
Administration route: Oral
Start date: 2007-07-01
End date: 2007-09-01
Contramal
Dosage: unknown
Administration route: Oral
Start date: 2007-07-01
End date: 2007-09-01
Other drugs received by patient: Levothyrox
Adverse event in male receiving Mobic (Meloxicam)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-19
Patient: male
Adverse reactions / side effects: Hepatic Failure, Hepatitis Fulminant
Adverse event resulted in: hospitalization
Suspect drug(s):
Contramal
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Mobic
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Effexor
Indication: Drug USE FOR Unknown Indication
Amlor
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Levothyroxine Sodium
Adverse event in 71 year old male receiving Mobic (Meloxicam)
Reported by a physician from Japan on 2007-10-19
Patient: 71 year old male, weighing 29.0 kg (63.8 pounds)
Adverse reactions / side effects: Arthritis Infective
Adverse event resulted in: hospitalization
Suspect drug(s):
Tacrolimus
Dosage: 1 mg, oral; 2 mg, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2005-05-13
End date: 2005-06-09
Tacrolimus
Dosage: 1 mg, oral; 2 mg, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
Start date: 2005-06-10
Mobic
Dosage: 10 mg, qod, oral
Administration route: Oral
Indication: Rheumatoid Arthritis
Adverse event in 73 year old female receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from Taiwan, Province of China on 2007-10-19
Patient: 73 year old female
Adverse reactions / side effects: Ileal Perforation, Atrial Fibrillation, Septic Shock, Peritonitis
Adverse event resulted in: death
Suspect drug(s):
Aspirin
Administration route: Oral
Indication: Cardiovascular Event Prophylaxis
Start date: 2003-05-20
End date: 2007-10-03
Telmisartan
Administration route: Oral
Indication: Hypertension
Start date: 2007-08-10
End date: 2007-10-03
Cortisone Acetate
Administration route: Oral
Indication: Adrenal Insufficiency
Start date: 2007-04-06
End date: 2007-10-03
Mobic
Administration route: Oral
Indication: Sciatica
Start date: 2007-09-12
End date: 2007-10-03
Flurbiprofen
Administration route: Oral
Indication: Back Pain
Start date: 2007-05-21
End date: 2007-10-03
Other drugs received by patient: Levothyroxine Sodium; Theophyliline; Lercanidipine; Bisoprolol Fumarate; Amiodarone HCL; Bumetanide
Adverse event in 75 year old female receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from United States on 2007-10-17
Patient: 75 year old female
Adverse reactions / side effects: Transient Ischaemic Attack
Suspect drug(s):
Mobic
Indication: Osteoarthritis
Start date: 2007-02-06
End date: 2007-02-13
Mobic
Start date: 2007-02-13
End date: 2007-09-19
Study Drug
Indication: Osteoarthritis
Start date: 2007-01-22
End date: 2007-09-19
Other drugs received by patient: Benazepril Hydrochloride; Crestor; Alphagan; Nasonex; Travatan; Multi-Vitamin; Vitamin B-12
Adverse event in 55 year old male receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from United States on 2007-10-17
Patient: 55 year old male
Adverse reactions / side effects: Arterial Occlusive Disease, Transient Ischaemic Attack
Adverse event resulted in: hospitalization
Suspect drug(s):
Mobic
Indication: Osteoarthritis
Start date: 2007-08-23
Study Drug
Indication: Osteoarthritis
Other drugs received by patient: Loratadine; Cetirizine+pseudoephedrine
Adverse event in 58 year old female receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-15
Patient: 58 year old female, weighing 54.4 kg (119.7 pounds)
Adverse reactions / side effects: Aphthous Stomatitis
Suspect drug(s):
Lunesta
Dosage: 2 mg;prn;oral
Administration route: Oral
Indication: Insomnia
Start date: 2007-01-01
Lyrica
Indication: Nerve Injury
Start date: 2007-01-01
Mobic
Indication: Inflammation
Start date: 2007-01-01
Adverse event in female receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-12
Patient: female
Adverse reactions / side effects: Hypersensitivity, DRY Mouth, Sneezing, Nasal Dryness
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Inflammation
Start date: 2007-09-02
Mobic
Indication: Pain
Adverse event in receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-12
Patient:
Adverse reactions / side effects: Gastrointestinal Perforation
Adverse event resulted in: death
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in female receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-12
Patient: female
Adverse reactions / side effects: Fatigue, Palpitations, Arthralgia, Gastroenteritis Viral
Suspect drug(s):
Mobic (Meloxicam)
Other drugs received by patient: Theophylline; Hyzaar; Synthroid; Allegra D 24 Hour; Allopurinol; Alupent; Advair Diskus 100 / 50
Adverse event in 49 year old female receiving Mobic (Meloxicam)
Reported by a individual with unspecified qualification from United States on 2007-10-10
Patient: 49 year old female
Adverse reactions / side effects: Bladder Prolapse, Haematocrit Decreased, Haemorrhage, Post Procedural Haemorrhage
Adverse event resulted in: hospitalization
Suspect drug(s):
Mobic
Administration route: Oral
Indication: Arthralgia
Start date: 2007-01-12
End date: 2007-06-19
Unknown Study Drug
Indication: Arthralgia
Start date: 2006-12-28
End date: 2007-07-09
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-08
Patient: female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Gastric Ulcer Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-08
Patient: female
Adverse reactions / side effects: Haemorrhage, Haematoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Mobic
Administration route: Oral
Plavix
Administration route: Oral
Aspirin
Administration route: Oral
Other drugs received by patient: Avapro; Lanoxin; Norvasc
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-04
Patient: female, weighing 45.0 kg (99.0 pounds)
Adverse reactions / side effects: Haemoptysis, Gastric Ulcer Haemorrhage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from Australia on 2007-10-03
Patient: female
Adverse reactions / side effects: Haemorrhage, Haematoma
Adverse event resulted in: hospitalization
Suspect drug(s):
Mobic
Administration route: Oral
Plavix
Administration route: Oral
Aspirin
Administration route: Oral
Other drugs received by patient: Avapro; Lanoxin; Norvasc
Adverse event in 57 year old male receiving Mobic (Meloxicam)
Reported by a consumer/non-health professional from United States on 2007-10-02
Patient: 57 year old male, weighing 108.0 kg (237.5 pounds)
Adverse reactions / side effects: Toxic Epidermal Necrolysis, Pharyngitis Streptococcal, Scar, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Mobic (Meloxicam)
Adverse event in 67 year old female receiving Mobic (Meloxicam)
Reported by a physician from Japan on 2007-10-01
Patient: 67 year old female
Adverse reactions / side effects: Gingivitis, Pneumocystis Jiroveci Infection, Pneumonia Cytomegaloviral
Adverse event resulted in: hospitalization
Suspect drug(s):
Adalat
Administration route: Oral
Remicade
Indication: Rheumatoid Arthritis
Start date: 2004-10-21
Remicade
Start date: 2004-11-18
Rheumatrex
Rimatil
Administration route: Oral
Mobic
Mucosta
Administration route: Oral
Baylotensin
Administration route: Oral
Dibetos
Administration route: Oral
Catapres
Administration route: Oral
Glimicron
Administration route: Oral
Basen
Administration route: Oral
Methycobal
Administration route: Oral
Lipitor
Administration route: Oral
Other drugs received by patient: Predonine; Predonine; Predonine; Predonine; Predonine; Predonine; Predonine; Predonine; NU-Lotan; Insulin; Famotidine; Fangizone; Isodine; Diart; Clarithromycin; Ketoprofen; Simavastatin; Urso 250
Adverse event in female receiving Mobic (Meloxicam)
Reported by a physician from United States on 2007-10-01
Patient: female, weighing 118.8 kg (261.5 pounds)
Adverse reactions / side effects: Drug Toxicity, Atrial Fibrillation, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyflo
Dosage: (df)
Indication: Asthma
Start date: 2007-02-01
End date: 2007-02-01
Zyflo
Dosage: (df)
Indication: Status Asthmaticus
Start date: 2007-02-01
End date: 2007-02-01
Diovan
Dosage: (160 mg qd oral), (160 mg qd oral), (320 mg qd oral)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2007-02-01
Diovan
Dosage: (160 mg qd oral), (160 mg qd oral), (320 mg qd oral)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-04-09
End date: 2007-06-15
Diovan
Dosage: (160 mg qd oral), (160 mg qd oral), (320 mg qd oral)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-06-15
Benazepril HCL
Dosage: (40 mg bid), (40 mg qd)
Indication: Drug USE FOR Unknown Indication
End date: 2007-02-01
Mobic
Dosage: (7.5 mg, 1 dose qd prn)
Indication: Arthralgia
End date: 2007-02-01
Coumadin
Dosage: (3 mg 4x/week), (5 mg 3x/week)
Indication: Atrial Fibrillation
Prednisone
Other drugs received by patient: Toprol-XL; Avandia; Singulair; Quinine Sulfate; Advair Diskus 100 / 50; Protonix; Lipitor; Spiriva; Combivent; Alprazolam; Glucophage; Lasix; Cardizem CD; Melatonin; Ambien; Potassium Chloride; Insulin; Rhinocort; Macrobid; Wellbutrin; Theophylline; Multi-Vitamin; Nitroglycerin; Magnesium Sulfate; Hormones NOS; Lexapro; Aspirin
Adverse event in 55 year old female receiving Mobic (Meloxicam)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-07-31
Patient: 55 year old female
Adverse reactions / side effects: Vomiting, Anaemia, Faeces Discoloured, Haematemesis, Haemoglobin Decreased, Diarrhoea, C-Reactive Protein Increased, Bacterial DNA Test Positive, Duodenal Ulcer Haemorrhage, Melaena, White Blood Cell Count Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Voltaren
Dosage: 50 mg, tid
Indication: Back Pain
Start date: 2007-01-01
End date: 2007-07-10
Mobic
Dosage: 15 mg, bid
Administration route: Oral
End date: 2007-07-10
Other drugs received by patient: Surmontil; Paralgin Forte; Sobril; Sumatriptan Succinate
Adverse event in 70 year old male receiving Mobic (Meloxicam)
Reported by a physician from Japan on 2007-07-31
Patient: 70 year old male, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Sepsis, Liver Disorder, Stevens-Johnson Syndrome
Adverse event resulted in: death
Suspect drug(s):
Naproxen
Administration route: Oral
Indication: Pyrexia
Start date: 2006-09-20
End date: 2006-09-26
Rohypnol
Administration route: Oral
Start date: 2006-09-13
End date: 2006-09-15
Rohypnol
Administration route: Oral
Start date: 2006-09-18
End date: 2006-09-19
Rohypnol
Administration route: Oral
Start date: 2006-09-21
End date: 2006-09-21
Rohypnol
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-26
Cercine
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-09-24
End date: 2006-09-26
Perdipine
Dosage: dose increased or decreased based on blood pressure, on an as needed basis
Indication: Hypertension
Start date: 2006-08-24
End date: 2006-08-24
Amoban
Dosage: drug name: amoban tablets 7.5.
Administration route: Oral
Start date: 2006-09-20
End date: 2006-09-20
Amoban
Administration route: Oral
Start date: 2006-09-22
End date: 2006-09-23
Amoban
Administration route: Oral
Start date: 2006-09-25
End date: 2006-09-25
Magmitt
Administration route: Oral
Indication: Constipation
Start date: 2006-08-29
End date: 2006-09-26
Phenobarbital TAB
Administration route: Oral
Indication: Convulsion Prophylaxis
Start date: 2006-08-28
End date: 2006-09-23
Myslee
Administration route: Oral
Start date: 2006-08-22
End date: 2006-08-22
Myslee
Administration route: Oral
Start date: 2006-08-31
End date: 2006-08-31
Myslee
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-23
Ubretid
Administration route: Oral
Indication: Neurogenic Bladder
Start date: 2006-09-08
End date: 2006-09-29
Spelear
Administration route: Oral
Indication: Sputum Retention
Start date: 2006-09-14
End date: 2006-09-24
Selbex
Administration route: Oral
Indication: Gastritis
Start date: 2006-09-24
End date: 2006-09-24
Lansoprazole
Administration route: Oral
Indication: Gastric Ulcer
Start date: 2006-08-24
End date: 2006-08-24
Lansoprazole
Administration route: Oral
Start date: 2006-09-06
End date: 2006-09-29
Tegretol
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-22
End date: 2006-09-23
Aspirin
Administration route: Oral
Indication: Cerebral Infarction
Start date: 2006-08-30
End date: 2006-09-30
Polaramine
Administration route: Oral
Indication: Pruritus
Start date: 2006-09-23
End date: 2006-09-23
Loxonin
Administration route: Oral
Indication: Wound Complication
Start date: 2006-09-18
End date: 2006-09-20
Loxonin
Administration route: Oral
Start date: 2006-09-23
End date: 2006-09-24
Voltaren
Indication: Wound Complication
Start date: 2006-08-24
End date: 2006-08-24
Voltaren
Dosage: form: rectal suppository.
Start date: 2006-09-04
Voltaren
Start date: 2006-09-17
End date: 2006-09-17
Voltaren
Start date: 2006-09-18
End date: 2006-09-19
Voltaren
Start date: 2006-09-20
End date: 2006-09-22
Voltaren
Start date: 2006-09-23
End date: 2006-09-23
Ketoprofen
Dosage: form: tape. dose: adjusted 10 x 14 cm.
Indication: Wound Complication
Start date: 2006-09-17
Laxoberon
Dosage: dose: as needed
Administration route: Oral
Indication: Constipation
Start date: 2006-09-02
Rinderon-VG
Dosage: dose: as needed
Administration route: Topical
Indication: Rash
Start date: 2006-09-18
Solu-Medrol
Indication: Asthma
Start date: 2006-09-20
End date: 2006-09-21
Aminofluid
Indication: Fluid Replacement
Start date: 2006-09-25
End date: 2006-09-26
Pasil
Indication: Infection
Start date: 2006-09-20
End date: 2006-09-20
Finibax
Indication: Infection
Start date: 2006-09-19
End date: 2006-09-20
Flumarin
Indication: Infection
Start date: 2006-09-17
End date: 2006-09-17
NEO-Minophagen C
Indication: Hepatic Function Abnormal
Start date: 2006-09-01
End date: 2006-09-11
NEO-Minophagen C
Start date: 2006-09-25
End date: 2006-09-27
NEO-Minophagen C
Start date: 2006-09-29
End date: 2006-10-12
Sennoside
Administration route: Oral
Indication: Constipation
Start date: 2006-08-22
End date: 2006-08-22
Humulin 70 / 30
Indication: Hyperglycaemia
Start date: 2006-08-23
End date: 2006-08-24
Mobic
Administration route: Oral
Start date: 2006-08-24
End date: 2006-08-24
Albumin (Human)
Start date: 2006-08-24
End date: 2006-08-24
1 Suspected Drug
Dosage: drug name reported as anapeine (ropivacaine)
Start date: 2006-08-24
End date: 2006-08-26
Omeprazole
Start date: 2006-08-24
End date: 2006-08-30
1 Suspected Drug
Dosage: drug name reported as pansporin (cefotiam hydrochloride)
Indication: Infection Prophylaxis
Start date: 2006-08-24
End date: 2006-08-26
Cataclot
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-08-24
Multivitamin Additive
Dosage: total daily dose =1 vial
Indication: Vitamin Supplementation
Start date: 2006-08-24
End date: 2006-08-30
Novo-Heparin
Indication: Drug USE FOR Unknown Indication
Start date: 2006-08-24
End date: 2006-08-27
Bisolvon
Dosage: taken on an as needed basis
Start date: 2006-08-24
End date: 2006-08-24
Bisolvon
Dosage: taken on an as needed basis
Start date: 2006-08-29
End date: 2006-09-04
Radicut
Indication: Cerebral Infarction
Start date: 2006-08-24
End date: 2006-09-03
Amino Acid INJ
Indication: Nutritional Support
Start date: 2006-08-24
End date: 2006-08-25
Other drugs received by patient: Unspecified Drug
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