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Lanoxin (Digoxin) - Adverse Event Reports - Life Threatening Events

 



Index of reports > Cases resulting in life threatening events (4)

     Long QT Syndrome (2)Torsade DE Pointes (2)Syncope (2)Confusional State (1)Nausea (1)Fatigue (1)Poisoning (1)Depression (1)Pharmaceutical Product Complaint (1)Renal Failure Acute (1)

Below is the selection of adverse event reports related to Lanoxin (Digoxin) that includes cases resulting in life threatening events.

Adverse event in female receiving Lanoxin (Digoxin)

Reported by a individual with unspecified qualification from United States on 2007-10-24

Patient: female, weighing 47.2 kg (103.8 pounds)

Adverse reactions / side effects: Weight Decreased, Confusional State, Vomiting, Nausea, Fatigue, Syncope, Diarrhoea, Anorexia, Poisoning, Depression, Pharmaceutical Product Complaint, Decreased Appetite

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lanoxin (Digoxin)



Adverse event in receiving Lanoxin (Digoxin)

Reported by a individual with unspecified qualification from Italy on 2007-05-25

Patient:

Adverse reactions / side effects: Hypovolaemic Shock, Therapeutic Agent Toxicity, Drug Interaction, Bradycardia, Renal Failure Acute

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Lanoxin (Digoxin)

Other drugs received by patient possibly interacting with the suspect drug:
Altace
    Dosage: 2.5 mg, qd
    Administration route: Oral
    Indication: Myocardial Infarction
    Start date: 2007-02-28
    End date: 2007-04-26

Lasix
    Dosage: 25 mg, qd
    Administration route: Oral
    Indication: Myocardial Infarction
    Start date: 2007-02-28
    End date: 2007-04-26

Luvion / 00252501 /
    Dosage: 50 mg, qod
    Administration route: Oral
    Indication: Myocardial Infarction
    Start date: 2007-02-01
    End date: 2007-04-26

Other drugs received by patient: Deltacortene; Antra / 00661201 /; Indobufen; Congescor



Adverse event in 67 year old receiving Lanoxin (Digoxin)

Reported by a individual with unspecified qualification from Canada on 2007-05-11

Patient: 67 year old

Adverse reactions / side effects: Torsade DE Pointes, Long QT Syndrome

Adverse event resulted in: life threatening event

Suspect drug(s):
Ciprofloxacin HCL (Formulation Unknown) (Ciprofloxacin Hcl) (Generic)
    Dosage: 500 mg / twice per day / oral
    Administration route: Oral
    Indication: Urinary Tract Infection

Amiodarone HCL
    Dosage: 400 mg / twice per day / oral
    Administration route: Oral
    Indication: Drug USE FOR Unknown Indication

Lanoxin
    Indication: Drug USE FOR Unknown Indication

Warfarin Sodium
    Indication: Drug USE FOR Unknown Indication



Adverse event in 44 year old female receiving Lanoxin (Digoxin)

Reported by a consumer/non-health professional from Canada on 2007-05-11

Patient: 44 year old female

Adverse reactions / side effects: Torsade DE Pointes, Syncope, Presyncope, Long QT Syndrome

Adverse event resulted in: life threatening event

Suspect drug(s):
Ciprofloxacin HCL (Formulation Unknown) (Ciprofloxacin Hcl) (Generic)
    Dosage: oral
    Administration route: Oral
    Indication: Pyelonephritis

Sotalol HCL
    Dosage: 160 mg / twice per day / oral
    Administration route: Oral
    Indication: Atrial Fibrillation

Lanoxin
    Indication: Drug USE FOR Unknown Indication

Warfarin Sodium
    Indication: Drug USE FOR Unknown Indication

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