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Ranitidine (Ranitidine) - Adverse Event Reports - Hospitalization - Dyspnoea

 



Index of reports > Cases resulting in hospitalization (49) > Cases with Dyspnoea (5)

Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in hospitalization where reactions include dyspnoea.

Adverse event in 39 year old female receiving Ranitidine

Reported by a consumer/non-health professional from Spain on 2007-06-29

Patient: 39 year old female

Adverse reactions / side effects: Dyspnoea, Dysphagia, Chest Pain

Adverse event resulted in: hospitalization

Suspect drug(s):
Taxol
    Indication: Neoplasm Malignant
    Start date: 2006-05-10
    End date: 2006-05-10

Cisplatin
    Indication: Neoplasm Malignant
    Start date: 2006-05-10
    End date: 2006-05-10

Ranitidine
    Indication: Neoplasm Malignant
    Start date: 2006-05-10
    End date: 2006-05-10



Adverse event in 75 year old female receiving Ranitidine

Reported by a individual with unspecified qualification from France on 2007-02-15

Patient: 75 year old female, weighing 110.0 kg (242.0 pounds)

Adverse reactions / side effects: Arrhythmia Supraventricular, Dyspnoea, Tongue Disorder, Macroglossia, Atrial Fibrillation, Laryngeal Oedema, Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Allopurinol Sodium
    Dosage: 1 df, qd
    Administration route: Oral
    End date: 2006-10-30

Bipreterax
    Dosage: 1 df, qd
    Administration route: Oral
    Start date: 2005-09-01
    End date: 2006-10-30

Ranitidine
    Dosage: 50 mg per day
    Administration route: Oral
    End date: 2006-10-30

Triatec
    Dosage: 5 mg, qd
    Administration route: Oral

Acarbose
    Dosage: 50 mg, qd
    Administration route: Oral

Tareg
    Dosage: 80 mg, qd
    Administration route: Oral
    End date: 2006-10-30

Other drugs received by patient: Lasix; Diamicron; Aspegic 1000



Adverse event in receiving Ranitidine

Reported by a consumer/non-health professional from United States on 2007-02-13

Patient:

Adverse reactions / side effects: Atrial Tachycardia, Dyspnoea, Tongue Oedema, Atrial Fibrillation, Laryngeal Oedema

Adverse event resulted in: hospitalization

Suspect drug(s):
Altace
    Dosage: 5 mg, qd
    Administration route: Oral
    End date: 2006-10-30

Altace
    Start date: 2006-11-01

Acarbose
    Dosage: 50 mg, qd
    Administration route: Oral
    End date: 2006-10-30

Allopurinol Sodium
    Dosage: 1 u, qd
    Administration route: Oral
    End date: 2006-10-30

Tareg
    Dosage: 80 mg, qd
    Administration route: Oral
    End date: 2006-10-30

Bipreterax
    Dosage: 1 u, qd
    Start date: 2005-09-01
    End date: 2006-10-30

Ranitidine
    Dosage: 50 mg, qd
    Administration route: Oral
    End date: 2006-10-30

Other drugs received by patient: Lasilix / 00032601 /; Diamicron; Aspegic / 00657701 /



Adverse event in 75 year old female receiving Ranitidine

Reported by a physician from France on 2007-01-30

Patient: 75 year old female, weighing 110.0 kg (242.0 pounds)

Adverse reactions / side effects: Dyspnoea, Allergic Oedema, Tongue Oedema, Atrial Fibrillation, Laryngeal Oedema, Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Acarbose
    Dosage: total daily dose: 50 mg unit dose: 50 mg
    Administration route: Oral
    Indication: Diabetes Mellitus

Allopurinol Sodium
    Administration route: Oral
    Indication: Hyperuricaemia
    End date: 2006-10-30

Tareg
    Administration route: Oral
    Indication: Hypertension
    End date: 2006-10-30

Bipreterax
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-09-01
    End date: 2006-10-30

Ranitidine
    Administration route: Oral
    Indication: Unevaluable Event
    End date: 2006-10-30

Triatec
    Dosage: total daily dose: 5 mg unit dose: 5 mg
    Administration route: Oral
    Indication: Hypertension

Other drugs received by patient: Lasix; Diamicron; Aspegic 1000



Adverse event in 75 year old female receiving Ranitidine

Reported by a physician from France on 2007-01-17

Patient: 75 year old female, weighing 110.0 kg (242.0 pounds)

Adverse reactions / side effects: Dyspnoea, Allergic Oedema, Tongue Oedema, Laryngeal Oedema

Adverse event resulted in: hospitalization

Suspect drug(s):
Acarbose
    Dosage: total daily dose: 50 mg unit dose: 50 mg
    Administration route: Oral
    Indication: Diabetes Mellitus

Allopurinol Sodium
    Administration route: Oral
    Indication: Hyperuricaemia

Tareg
    Administration route: Oral
    Indication: Hypertension

Bipreterax
    Administration route: Oral
    Indication: Hypertension
    Start date: 2005-09-01

Ranitidine
    Administration route: Oral
    Indication: Unevaluable Event

Triatec
    Dosage: total daily dose: 5 mg unit dose: 5 mg
    Administration route: Oral
    Indication: Hypertension

Other drugs received by patient: Lasix; Diamicron; Aspegic 1000

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