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Voltaren-XR (Diclofenac Extended Release) - Reports of Side Effects & Adverse Reactions

 


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This is an index of adverse event reports related to Voltaren-XR (Diclofenac Extended Release). 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 adverse reaction. Or scroll down to view all available reports.

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 (2)
     Dyspnoea (1)Pain in Extremity (1)Cerebrovascular Accident (1)more >>

Cases resulting in a serious event (2)
     Dyspnoea (1)Pain in Extremity (1)Cerebrovascular Accident (1)more >>

Cases resulting in hospitalization (2)
     Dyspnoea (1)Pain in Extremity (1)Cerebrovascular Accident (1)more >>

Cases resulting in other serious reactions (1)
     Dyspnoea (1)Drug Ineffective (1)Cerebrovascular Accident (1)more >>

Adverse event in 71 year old female receiving Voltaren-XR (Diclofenac Extended Release)

Reported by a health professional (non-physician/pharmacist) from France on 2007-04-20

Patient: 71 year old female

Adverse reactions / side effects: Bone Lesion, Pain in Extremity, Wound Infection, Erythema, Osteitis, Joint Destruction, Wound Secretion, Nuclear Magnetic Resonance Imaging Abnormal, Leukocytosis, RED Blood Cell Sedimentation Rate Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Arava
    Administration route: Oral
    Start date: 2004-06-15

Cortancyl
    Administration route: Oral

Enbrel
    Dosage: 50 mg total weekly
    Indication: Polyarthritis
    Start date: 2005-03-15
    End date: 2007-03-06

Voltaren-XR
    Administration route: Oral
    End date: 2007-03-09

Other drugs received by patient: Nexium



Adverse event in male receiving Voltaren-XR (Diclofenac Extended Release)

Reported by a physician from United States on 2007-03-06

Patient: male, weighing 97.5 kg (214.5 pounds)

Adverse reactions / side effects: Dyspnoea, Drug Ineffective, Cerebrovascular Accident, Convulsion, Malaise, Diarrhoea Haemorrhagic, Oedema, Intracranial Aneurysm, Upper Gastrointestinal Haemorrhage

Adverse event resulted in: hospitalization

Suspect drug(s):
Arthrotec
    Administration route: Oral
    Indication: Arthritis
    Start date: 2001-10-01
    End date: 2006-12-18

Tegretol
    Administration route: Oral
    Indication: Convulsion

Voltaren-XR
    Administration route: Oral
    Indication: Pain
    Start date: 2006-05-16
    End date: 2006-06-01

Other drugs received by patient: Tylenol W / Codeine NO. 3; Vasotec; Norvasc; Montelukast Sodium; Advair Diskus 100 / 50; Albuterol; Lamictal; Pravachol; Lasix

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