DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Septra (Trimethoprim / Sulfamethoxazole) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (14)

     Hypersensitivity (2)Pruritus (2)Skin Exfoliation (2)Rash Erythematous (2)Abscess (2)Stevens-Johnson Syndrome (2)White Blood Cell Count Decreased (1)Febrile Neutropenia (1)Haematocrit Decreased (1)Arthralgia (1)

Below is the selection of adverse event reports related to Septra (Trimethoprim / Sulfamethoxazole) that includes cases resulting in hospitalization.

Adverse event in male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31

Patient: male, weighing 108.9 kg (239.5 pounds)

Adverse reactions / side effects: Tendon Rupture, Injury

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Cipro
    Dosage: 500mg bid po x 7 days
    Administration route: Oral
    Indication: Prostatomegaly
    Start date: 1999-08-01

Cipro
    Dosage: 500mg bid po x 7 days
    Administration route: Oral
    Indication: Urinary Tract Infection
    Start date: 1999-08-01

Cipro
    Dosage: 500mg bid po x 21 days
    Administration route: Oral
    Indication: Prostatitis
    Start date: 2001-03-01

Cipro
    Dosage: 500 bid x 21 days
    Indication: Prostatitis
    Start date: 1999-08-12

Septra
    Dosage: bid
    Start date: 1999-07-20
    End date: 1999-07-29



Adverse event in 43 year old female receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a physician from United States on 2007-07-25

Patient: 43 year old female, weighing 84.4 kg (185.6 pounds)

Adverse reactions / side effects: Incision Site Pain, Cellulitis, Febrile Neutropenia, Abscess

Adverse event resulted in: hospitalization

Suspect drug(s):
PEG-Intron
    Dosage: 0.48 ml; qw; sc
    Indication: Hepatitis C
    Start date: 2006-02-03
    End date: 2007-01-04

Rebetol
    Dosage: 1200 mg; qd; po
    Administration route: Oral
    Indication: Hepatitis C
    Start date: 2006-02-03
    End date: 2007-01-04

Septra
    Indication: Abscess
    Start date: 2007-01-09
    End date: 2007-01-28

Septra
    Indication: Cellulitis
    Start date: 2007-01-09
    End date: 2007-01-28

Other drugs received by patient: Effexor; Prevacid; Phenergan HCL



Adverse event in receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a pharmacist from United States on 2007-06-29

Patient:

Adverse reactions / side effects: Brain Death, Confusional State, Nervous System Disorder, Brain Oedema, Delirium, CSF Protein

Adverse event resulted in: death, hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)



Adverse event in 74 year old male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a pharmacist from United States on 2007-06-20

Patient: 74 year old male

Adverse reactions / side effects: Myalgia, Dysstasia, Hyperkalaemia, Abasia, Muscular Weakness

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra
    Dosage: 1 tab bid po
    Administration route: Oral
    Indication: Cellulitis
    Start date: 2007-06-01
    End date: 2007-06-09

Septra
    Dosage: 1 tab bid po
    Administration route: Oral
    Indication: Skin Infection
    Start date: 2007-06-01
    End date: 2007-06-09



Adverse event in 9 year old male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-07

Patient: 9 year old male, weighing 45.4 kg (99.8 pounds)

Adverse reactions / side effects: Toxic Epidermal Necrolysis, Stevens-Johnson Syndrome

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)



Adverse event in male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a pharmacist from United States on 2007-05-15

Patient: male, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Secondary Syphilis, Stevens-Johnson Syndrome

Adverse event resulted in: hospitalization

Suspect drug(s):
Doxycycline
    Dosage: 100 mg po
    Administration route: Oral
    Indication: Secondary Syphilis
    Start date: 2007-04-09
    End date: 2007-04-23

Septra
    Indication: Secondary Syphilis
    Start date: 2007-04-10
    End date: 2007-04-23



Adverse event in 50 year old male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a physician from United States on 2007-04-26

Patient: 50 year old male, weighing 79.1 kg (174.0 pounds)

Adverse reactions / side effects: Drug Eruption, Lymphadenopathy, Skin Exfoliation, Drug Hypersensitivity, Penile Swelling, Groin Pain, Muscle Strain, Arthralgia, Rash Erythematous, Penis Disorder, Abscess, Purulent Discharge, Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)

Other drugs received by patient: Tylenol W / Codeine



Adverse event in 59 year old male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a physician from United States on 2007-04-26

Patient: 59 year old male, weighing 104.3 kg (229.5 pounds)

Adverse reactions / side effects: Pruritus, Renal Failure Acute, Rash Macular

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)

Other drugs received by patient: Haldol; Terazosin HCL; Lorazepam; Metformin HCL; Atenolol; Simvastatin; Glyburide; Salsalate; Clopidogrel; Warfarin Sodium; Benztropine; Divalproex Sodium



Adverse event in receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a consumer/non-health professional from United States on 2007-04-05

Patient:

Adverse reactions / side effects: Productive Cough, Blood Bilirubin Increased, Hepatic Failure, Pyrexia, Prothrombin Time Prolonged, Idiosyncratic Drug Reaction, Cardiopulmonary Failure, Blood Creatinine Increased, Blood Alkaline Phosphatase Increased, Metabolic Alkalosis, Hypotension, Blood Lactate Dehydrogenase Increased, Chromaturia, Urine Bilirubin Increased, Hepatocellular Damage, Rash Erythematous, Aspartate Aminotransferase Increased, Rash Maculo-Papular, Jaundice, Hypersensitivity, Skin Exfoliation, Cholestasis, Abdominal Pain Upper, Hepatitis Cholestatic, Fatigue, Hepatomegaly, Gamma-Glutamyltransferase Increased, Thrombocytopenia, Splenomegaly, Oxygen Saturation Decreased, Vomiting, Alanine Aminotransferase Increased, Ascites, Acquired Diaphragmatic Eventration, Hypoalbuminaemia, Lung Infiltration, Leukopenia, RED Blood Cell Sedimentation Rate Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)



Adverse event in receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a physician from Japan on 2007-02-07

Patient:

Adverse reactions / side effects: Haemoglobin Decreased, White Blood Cell Count Decreased, Haematocrit Decreased, Anaemia, Platelet Count Decreased

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra
    Dosage: 1 tablet, qd
    Administration route: Oral
    Indication: Antifungal Prophylaxis
    Start date: 2005-07-01
    End date: 2005-07-11

Valganciclovir HCL
    Dosage: 900 mg, bid
    Administration route: Oral
    Indication: Cytomegalovirus Enterocolitis
    Start date: 2005-07-29
    End date: 2005-08-18

Valganciclovir HCL
    Dosage: 900 mg, qd
    Start date: 2005-10-08

Zidovudine
    Dosage: 400 mg, qd
    Administration route: Oral
    Indication: Acquired Immunodeficiency Syndrome
    Start date: 2005-07-01
    End date: 2005-09-07

Other drugs received by patient: Lamivudine; Ritonavir; Kaletra; Atazanavir; Tenofovir Disoproxil Fumarate; Adenosine Triphosphate



Adverse event in 23 year old male receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a individual with unspecified qualification from United States on 2007-01-30

Patient: 23 year old male

Adverse reactions / side effects: Drug Toxicity, Hepatitis, Rash Pruritic

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)



Adverse event in receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a consumer/non-health professional from Germany on 2007-01-29

Patient:

Adverse reactions / side effects: Agitation, Abnormal Behaviour, Hallucinations, Mixed, Psychotic Disorder, Thinking Abnormal, Mood Altered, Disturbance in Attention, Inappropriate Affect, Delusional Perception

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)

Other drugs received by patient: Opipramol



Adverse event in 34 year old female receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a pharmacist from United States on 2007-01-25

Patient: 34 year old female, weighing 54.0 kg (118.8 pounds)

Adverse reactions / side effects: Pharyngeal Oedema, Dyspnoea, Hypersensitivity, Pruritus, Rash

Adverse event resulted in: hospitalization

Suspect drug(s):
Septra (Trimethoprim / Sulfamethoxazole)



Adverse event in receiving Septra (Trimethoprim / Sulfamethoxazole)

Reported by a physician from Netherlands on 2007-01-12

Patient:

Adverse reactions / side effects: Hyponatraemia, Hypokalaemia

Adverse event resulted in: hospitalization

Suspect drug(s):
Altace
    Dosage: 5 mg, qd
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-02
    End date: 2006-07-21

Hydrochlorothiazide
    Dosage: 25 mg, qd
    Administration route: Oral
    Indication: Hypertension
    Start date: 2006-02-02
    End date: 2006-07-21

Septra
    Administration route: Oral
    Indication: Urinary Tract Infection
    Start date: 2006-07-01
    End date: 2006-07-21

Other drugs received by patient: Atenololum; Simvastatin; Calcium Carbonate; Fosamax

-- advertisement -- The American Red Cross
We comply with
HONcode standard.
Verify here.
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2009