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Tagamet (Cimetidine) - Adverse Event Reports - Serious Event - Toxic Epidermal Necrolysis

 



Index of reports > Cases resulting in a serious event (23) > Cases with Toxic Epidermal Necrolysis (4)

Below is the selection of adverse event reports related to Tagamet (Cimetidine) that includes cases resulting in a serious event where reactions include toxic epidermal necrolysis.

Adverse event in 83 year old female receiving Tagamet (Cimetidine)

Reported by a physician from Japan on 2007-10-16

Patient: 83 year old female

Adverse reactions / side effects: Multi-Organ Failure, Dialysis, Disseminated Intravascular Coagulation, Rash Papular, Condition Aggravated, Toxic Epidermal Necrolysis, Altered State of Consciousness, Renal Failure Acute

Adverse event resulted in: death, life threatening event

Suspect drug(s):
Baktar (Sulfamethoxazole / Trimethoprim) (NO Pref. Name)
    Dosage: 2 df, qd; po
    Administration route: Oral
    Indication: Pneumocystis Jiroveci Pneumonia
    Start date: 2006-06-17
    End date: 2006-09-14

Rinderon-VG (Betamethasone Valerate / Gentamicin Sulfate) (Betamethasone
    Dosage: 10 mg, qd
    Indication: Dermatitis Contact
    Start date: 2006-09-12
    End date: 2006-09-14

Stromectol (Overmectin) (NO Pref. Name)
    Dosage: 9 mg, qd; po
    Administration route: Oral
    Indication: Acarodermatitis
    Start date: 2006-09-05
    End date: 2006-09-05

Tagamet
    Dosage: 400 mg;qd;po
    Administration route: Oral
    Indication: Gastritis
    Start date: 2006-01-31
    End date: 2006-09-14

Other drugs received by patient: Basen; Norvasc; Prednisolone; Eurax



Adverse event in 83 year old female receiving Tagamet (Cimetidine)

Reported by a physician from Japan on 2007-10-11

Patient: 83 year old female

Adverse reactions / side effects: Multi-Organ Failure, Disseminated Intravascular Coagulation, Toxic Epidermal Necrolysis

Adverse event resulted in: death

Suspect drug(s):
Baktar
    Administration route: Oral
    Indication: Pneumocystis Jiroveci Pneumonia
    Start date: 2006-05-17
    End date: 2006-09-14

Stromectol
    Administration route: Oral
    Indication: Acarodermatitis
    Start date: 2006-09-05
    End date: 2006-09-05

Tagamet
    Administration route: Oral
    Indication: Gastritis
    Start date: 2006-01-31
    End date: 2006-09-14

Other drugs received by patient: Basen; Norvasc; Prednisolone



Adverse event in 83 year old female receiving Tagamet (Cimetidine)

Reported by a consumer/non-health professional from Japan on 2007-10-11

Patient: 83 year old female

Adverse reactions / side effects: Pruritus, Disseminated Intravascular Coagulation, Rash Papular, Tongue Ulceration, Toxic Epidermal Necrolysis, Blood Potassium Increased, Rash, Skin Erosion, Acarodermatitis

Adverse event resulted in: death

Suspect drug(s):
Tagamet (Cimetidine)

Other drugs received by patient: Prednisolone; Norvasc; Basen; Baktar



Adverse event in 83 year old female receiving Tagamet (Cimetidine)

Reported by a physician from Japan on 2007-10-08

Patient: 83 year old female

Adverse reactions / side effects: Multi-Organ Failure, Disseminated Intravascular Coagulation, Toxic Epidermal Necrolysis

Adverse event resulted in: death

Suspect drug(s):
Stromectol
    Administration route: Oral
    Indication: Acarodermatitis
    Start date: 2006-09-05
    End date: 2006-09-05

Tagamet
    Administration route: Oral
    Indication: Gastritis
    Start date: 2006-01-31
    End date: 2006-09-14

Other drugs received by patient: Basen; Norvasc; Prednisolone; Baktar

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