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Mobic (Meloxicam) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (71)

     Haemorrhage (6)Chest Pain (6)Diarrhoea (5)Metabolic Acidosis (4)Anaemia (4)Hepatitis (4)Haematochezia (4)Renal Impairment (4)Dizziness (4)Renal Failure Acute (4)

Below is the selection of adverse event reports related to Mobic (Meloxicam) that includes cases resulting in hospitalization.

 Reports 1 - 25 of 71   Next >>

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 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 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 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 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 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 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 60 year old female receiving Mobic (Meloxicam)

Reported by a physician from Japan on 2007-07-31

Patient: 60 year old female

Adverse reactions / side effects: Agranulocytosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Mobic
    Administration route: Oral
    Indication: Musculoskeletal Pain

Bepricor
    Administration route: Oral
    Indication: Tachycardia
    Start date: 2007-07-18
    End date: 2007-07-26

Methotrexate Sodium
    Administration route: Oral



Adverse event in 72 year old male receiving Mobic (Meloxicam)

Reported by a individual with unspecified qualification from United States on 2007-07-27

Patient: 72 year old male

Adverse reactions / side effects: Dizziness Exertional, Coronary Artery Disease, Procedural Dizziness

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Mobic
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2007-04-17

Mobic

Other drugs received by patient: Glucosamine and Chondroitin; Alka Seltzer; Tums; Claritin; Bisacodyl; Tylenol (Caplet); Imodium



Adverse event in male receiving Mobic (Meloxicam)

Reported by a physician from Australia on 2007-07-27

Patient: male, weighing 82.0 kg (180.4 pounds)

Adverse reactions / side effects: Gastrointestinal Haemorrhage

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Mobic
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2004-10-01
    End date: 2007-06-01

Cartia XT
    Administration route: Oral
    Indication: Prophylaxis

Other drugs received by patient: Augmentin Forte (Amoxycillin)



Adverse event in receiving Mobic (Meloxicam)

Reported by a physician from Australia on 2007-07-26

Patient:

Adverse reactions / side effects: Rectal Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Mobic (Meloxicam)



Adverse event in 81 year old male receiving Mobic (Meloxicam)

Reported by a pharmacist from United States on 2007-07-24

Patient: 81 year old male

Adverse reactions / side effects: Duodenal Ulcer, Upper Gastrointestinal Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Mobic

Aspirin

Other drugs received by patient: Zocor; Nadolol; Aricept; Zoloft



Adverse event in 69 year old male receiving Mobic (Meloxicam)

Reported by a physician from Australia on 2007-07-10

Patient: 69 year old male

Adverse reactions / side effects: Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Mobic (Meloxicam)

Other drugs received by patient: Astrix; Augmentin Forte (Amoxycillin)



Adverse event in 69 year old male receiving Mobic (Meloxicam)

Reported by a physician from Australia on 2007-07-06

Patient: 69 year old male

Adverse reactions / side effects: Polyp Colorectal, Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Mobic (Meloxicam)

Other drugs received by patient: Astrix; Augmentin Forte (Amoxycillin)



Adverse event in 73 year old female receiving Mobic (Meloxicam)

Reported by a individual with unspecified qualification from United States on 2007-07-02

Patient: 73 year old female

Adverse reactions / side effects: Abdominal Pain, Weight Decreased, Haemorrhoids, Rectal Haemorrhage, Headache, Diverticulum Intestinal, Cardiomegaly, Haematochezia, Diarrhoea, Blood Potassium Decreased, Arthralgia, Pleural Effusion, Lung Infiltration

Adverse event resulted in: hospitalization

Suspect drug(s):
Mobic
    Administration route: Oral
    Indication: Osteoarthritis
    Start date: 2007-04-26

Unspecified Study Drug
    Indication: Osteoarthritis
    Start date: 2007-04-12

Other drugs received by patient: Allegra; Flonase; Lisinopril; Chlorthalidone; Evista; Actos; Lyrica; Zanaflex; Lidoderm; Hydrocodone Bitartrate



Adverse event in male receiving Mobic (Meloxicam)

Reported by a physician from United States on 2007-06-28

Patient: male

Adverse reactions / side effects: Osteonecrosis

Adverse event resulted in: hospitalization

Suspect drug(s):
Enbrel
    Indication: Rheumatoid Arthritis
    Start date: 2004-01-01

Methotrexate
    Start date: 2006-10-01

Mobic
    Administration route: Oral
    Start date: 2006-10-01

Vicodin ES
    Start date: 2006-10-01

Zantac
    Start date: 2006-10-01

Lorazepam
    Start date: 2006-10-01



Adverse event in 69 year old female receiving Mobic (Meloxicam)

Reported by a health professional (non-physician/pharmacist) from Japan on 2007-06-08

Patient: 69 year old female

Adverse reactions / side effects: Interstitial Lung Disease

Adverse event resulted in: hospitalization

Suspect drug(s):
Taxol
    Indication: Uterine Cancer
    Start date: 2005-08-25
    End date: 2005-08-25

Paraplatin
    Indication: Uterine Cancer
    Start date: 2005-08-25
    End date: 2005-08-25

Mobic
    Administration route: Oral



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