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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Bactrim DS (Sulfamethoxazole / Trimethoprim). 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 side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
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 (77)
Cases resulting in a serious event (72)
Cases resulting in death (2)
Cases resulting in life threatening events (16)
Cases resulting in hospitalization (50)
Cases resulting in disability (9)
Cases resulting in other serious reactions (22)
Below is a sample of reports where side effects / adverse reactions may be related to Bactrim DS (Sulfamethoxazole / Trimethoprim). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 41 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-10-31
Patient: 41 year old male, weighing 77.6 kg (170.6 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Myalgia, Liver Function Test Abnormal, Pyrexia
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in 72 year old female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-10-29
Patient: 72 year old female, weighing 88.9 kg (195.6 pounds)
Adverse reactions / side effects: Respiratory Disorder, International Normalised Ratio Increased, Ataxia, Drug Interaction, Thrombocytopenia, Renal Failure Acute, Tremor
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS
Dosage: bid po
Administration route: Oral
Indication: Wound
Start date: 2007-09-17
End date: 2007-09-29
Sulfamethoxazole / Trimethoprim Unknown
Dosage: bid po
Administration route: Oral
Indication: Wound
Start date: 2007-10-03
End date: 2007-10-08
Adverse event in female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a health professional (non-physician/pharmacist) from Germany on 2007-10-26
Patient: female
Adverse reactions / side effects: Renal Failure, Bundle Branch Block Left
Adverse event resulted in: hospitalization
Suspect drug(s):
Inipomp
Administration route: Oral
End date: 2007-07-02
Aprovel
Administration route: Oral
Indication: Essential Hypertension
Vastarel
Administration route: Oral
Indication: Cardiac Disorder
End date: 2007-07-02
DI-Antalvic
Dosage: 'df^
Administration route: Oral
End date: 2007-07-02
Lansoyl
Dosage: ^df^
Administration route: Oral
Indication: Constipation
End date: 2007-07-02
Monuril
Dosage: 3 g frequency unspecified
Administration route: Oral
End date: 2007-07-02
Duragesic-100
Dosage: 25 ug 3/day
Start date: 2007-06-18
End date: 2007-06-29
Bactrim DS
Administration route: Oral
Start date: 2007-06-04
End date: 2007-06-20
Preterax
Administration route: Oral
Indication: Essential Hypertension
End date: 2007-07-02
Other drugs received by patient: Mediatensyl; Domperidone; Iperten; Nebivolol; Lasix; Nitroglycerin; Plavix; Voltaren; Lipanthyl ^fournier^; Acarbose; Flector; Dafalgan Codeine
Adverse event in 59 year old female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-10-26
Patient: 59 year old female, weighing 88.0 kg (193.6 pounds)
Adverse reactions / side effects: Glioblastoma Multiforme, Lymphopenia, Malignant Neoplasm Progression, Asthenia, Candidiasis, Cushing's Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Temozolomide
Dosage: 75 mg/m2;qd;po
Administration route: Oral
Indication: Glioblastoma Multiforme
Start date: 2007-07-01
End date: 2007-08-01
Temozolomide
Dosage: 75 mg/m2;qd;po
Administration route: Oral
Indication: Glioblastoma Multiforme
Start date: 2007-09-27
End date: 2007-10-01
Temozolomide
Bactrim DS
Dosage: tiw;po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Decadron
Dosage: 4 mg;qd;po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Keppra
Dosage: 500 mg;bid;po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Adverse event in female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a health professional (non-physician/pharmacist) from France on 2007-10-19
Patient: female
Adverse reactions / side effects: Hyperkalaemia
Adverse event resulted in: hospitalization
Suspect drug(s):
Duragesic-100
Indication: Drug USE FOR Unknown Indication
Start date: 2007-06-18
End date: 2007-06-29
Preterax
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Irbesartan
Indication: Drug USE FOR Unknown Indication
Vastarel
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Inipomp
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
DI Antalvic
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Lansoyl
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Monuril
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Bactrim DS
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-06-04
End date: 2007-06-20
Other drugs received by patient: Motilyo
Adverse event in 79 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a pharmacist from United States on 2007-10-18
Patient: 79 year old male, weighing 82.3 kg (181.1 pounds)
Adverse reactions / side effects: Hyperkalaemia, Renal Failure Acute, Arrhythmia
Adverse event resulted in: life threatening event
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in 94 year old female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-10-16
Patient: 94 year old female
Adverse reactions / side effects: Renal Failure, Blood Potassium Increased, Bundle Branch Block Left, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Monuril(fosfomycin Trometamol)
Dosage: 3 g po
Administration route: Oral
End date: 2007-07-02
Irbesartan
Dosage: 150 mg po
Administration route: Oral
Preterax
End date: 2007-07-02
Iperten(manidipne Hydrochloride)
Temerit (Nebivolol)
Lasix
Dosage: 20 mg
Mediatensyl (Urapidil)
Discortrine (Glyceryl Trinitrate)
Plavix
Vastarel (Trimetazidine)
Dosage: 35 mg qd po
Administration route: Oral
End date: 2007-07-02
Pantoprazole Sodium
Dosage: 20 mg po
Administration route: Oral
End date: 2007-07-02
DI-Antalvic
End date: 2007-07-02
Lansoyl (Parrafin, Liquid)
End date: 2007-07-02
Voltaren
Fenofibrate
Duragesic-100
Motilyo (Domperidone)
Acarbose
Bactrim DS
End date: 2007-07-02
Flector EP Gel (Diclofenac Epolaminum)
Dafalgan Codeine
Adverse event in 52 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from France on 2007-10-15
Patient: 52 year old male
Adverse reactions / side effects: Optic Neuritis Retrobulbar
Adverse event resulted in: disablity
Suspect drug(s):
Invirase
Dosage: reported dosing amount: 4 doses daily.
Start date: 2006-06-23
Invirase
Start date: 2002-03-18
Bactrim DS
Dosage: also received on 28 september 2005 and 23 june 2006.
Indication: Drug USE FOR Unknown Indication
Start date: 1998-10-27
Combivir
Dosage: reported dosing amount: 2 doses daily.
Start date: 2005-09-28
End date: 2006-06-23
Combivir
Start date: 1999-05-11
End date: 1999-08-01
Combivir
Start date: 2001-03-23
Telzir
Dosage: reported dosing amount: 2 doses daily. also received on 17 june 2005.
Start date: 2005-03-29
End date: 2006-06-23
Norvir
Dosage: also received on 15 october 2004, 29 march 2005, 28 september 2005, 17 june 2005 and 23 june 2006.
Start date: 2004-04-17
Norvir
Start date: 1999-09-21
Norvir
Start date: 2000-06-06
Norvir
Start date: 2001-03-23
Norvir
Start date: 2002-03-18
Neurontin
Indication: Trigeminal Neuralgia
Start date: 2006-01-01
Lyrica
Indication: Trigeminal Neuralgia
Start date: 2006-06-23
Retrovir
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-23
Retrovir
Start date: 2005-06-17
Viread
Indication: Drug USE FOR Unknown Indication
Start date: 2006-06-23
Viread
Start date: 2003-01-03
Viread
Start date: 2003-09-12
Viread
Start date: 2004-04-17
Viread
Start date: 2004-10-15
Viread
Start date: 2005-03-29
Viread
Start date: 2005-06-17
Other drugs received by patient: Sustiva; Videx; Videx; Videx; Zerit; Zerit; Zerit; Zerit; Hivid; Hivid; Crixivan; Crixivan; 1 Concomitant Drug; Epivir; Agenerase; Kaletra; Kaletra; Fuzeon; Fuzeon; 1 Concomitant Drug; 1 Concomitant Drug; Ziagen; Tercian; Laroxyl; Tenofovir
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-10-12
Patient: male, weighing 71.7 kg (157.8 pounds)
Adverse reactions / side effects: Normochromic Normocytic Anaemia, Renal Failure Acute, Gastritis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Atripla
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-02
End date: 2007-05-16
Bactrim DS
Administration route: Oral
Indication: Antifungal Prophylaxis
Start date: 2007-05-02
End date: 2007-05-16
Ibuprofen
Administration route: Oral
Indication: Arthralgia
Start date: 2007-04-16
End date: 2007-05-16
Other drugs received by patient: Kaletra; Fluconazole; Zofran; Azithromycin
Adverse event in 22 year old female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a pharmacist from United States on 2007-10-12
Patient: 22 year old female, weighing 60.0 kg (132.0 pounds)
Adverse reactions / side effects: Rash Generalised, Chills, Ocular Hyperaemia, Rash Erythematous, Pancytopenia, Eye Swelling
Adverse event resulted in: life threatening event
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-10
Patient: male, weighing 70.2 kg (154.4 pounds)
Adverse reactions / side effects: Blood Urea Increased, Blood Creatinine Increased
Suspect drug(s):
Bactrim DS
Dosage: 800/160mg bid po
Administration route: Oral
Indication: Abscess
Start date: 2007-08-24
End date: 2007-08-28
Bactrim DS
Dosage: 800/160mg bid po
Administration route: Oral
Indication: Cellulitis
Start date: 2007-08-24
End date: 2007-08-28
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-10
Patient: male, weighing 95.0 kg (209.0 pounds)
Adverse reactions / side effects: Renal Failure Acute, Cardiac Failure Congestive
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from France on 2007-10-09
Patient: male
Adverse reactions / side effects: Mononeuropathy Multiplex, Glaucoma, Optic Neuropathy, Trigeminal Neuralgia, Optic Neuritis Retrobulbar, Encephalopathy
Adverse event resulted in: disablity
Suspect drug(s):
Viread
Administration route: Oral
Indication: HIV Infection
Start date: 2002-03-18
Viread
Start date: 2006-06-23
Retrovir
Start date: 1992-01-01
End date: 1997-01-01
Retrovir
Start date: 2005-06-17
Bactrim
Start date: 1998-10-27
Combivir
Administration route: Oral
Indication: HIV Infection
Start date: 2000-09-01
End date: 2006-06-23
Norvir
Administration route: Oral
Indication: HIV Infection
Start date: 1999-09-21
Norvir
Administration route: Oral
Start date: 2004-04-17
Telzir
Administration route: Oral
Indication: HIV Infection
Start date: 2005-03-29
End date: 2006-06-23
Bactrim DS
Start date: 2002-03-18
Neurontin
Indication: Trigeminal Neuralgia
Start date: 2006-01-01
End date: 2006-07-20
Lyrica
Indication: Trigeminal Neuralgia
Start date: 2006-06-01
End date: 2006-07-20
Other drugs received by patient: Invirase; Invirase; Kaletra; Fuzeon; Reyataz; Ziagen; Tercian; Laroxyl
Adverse event in 47 year old female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-10-09
Patient: 47 year old female, weighing 68.7 kg (151.1 pounds)
Adverse reactions / side effects: White Blood Cell Count Decreased, Cellulitis, Haemorrhoids, Lymphopenia, Aplastic Anaemia, Bone Marrow Failure, Febrile Neutropenia, Thrombocytopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Temodar
Dosage: 75 mg/m2; qd; po
Administration route: Oral
Indication: Glioblastoma Multiforme
Start date: 2006-08-29
End date: 2006-09-25
Radiation Therapy
Dosage: qd
Indication: Glioblastoma Multiforme
Start date: 2006-08-29
End date: 2006-10-03
Bactrim DS
Dosage: 1 df tiw; po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
End date: 2006-10-20
Dexamethasone 0.5mg TAB
Indication: Drug USE FOR Unknown Indication
End date: 2006-10-01
Other drugs received by patient: Keppra; Prempro; Zofran; Rutovit C; Lycopene; Coq10; Shark-Liver OIL; Arnica Montana; Hamamelis Virginiana; Calcium Phosphate; Omega 3 Fish OIL; Ferrous Phosphate; M.v.i.; Ascorbic Acid; Vitamin D; Vitamin E; Vitamin B-12; Beta-Carotene Gisand; Flaxseed OIL
Adverse event in female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a individual with unspecified qualification from United States on 2007-10-05
Patient: female, weighing 103.0 kg (226.6 pounds)
Adverse reactions / side effects: Neuropathy, Febrile Neutropenia, Joint Injury, Fall, Tremor, Paraesthesia, Meniscus Lesion, Peroneal Nerve Palsy, Arthralgia, Staphylococcal Infection, Arthritis Infective, Hyporeflexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS
Dosage: 10000 mg
End date: 2007-08-29
Cyclophosphamide
Dosage: 2180 mg
End date: 2007-08-07
Cytarabine
Dosage: 13110 mg
End date: 2007-08-09
G-CSF (Filgrastim, Amgen)
Dosage: 5280 mg
End date: 2007-08-20
Methotrexate
Dosage: 15 mg
End date: 2007-08-07
Other drugs received by patient: Acyclovir; Compazine; Digoxin; Diltiazem CD; Levothyroxine Sodium; Potassium Chloride; Protonix; Zoloft
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a pharmacist from United States on 2007-10-02
Patient: male
Adverse reactions / side effects: Rash Erythematous, Rash Maculo-Papular
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in 24 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a individual with unspecified qualification from United States on 2007-07-31
Patient: 24 year old male, weighing 61.2 kg (134.7 pounds)
Adverse reactions / side effects: Refusal of Treatment by Patient, Drug Dose Omission, Vomiting, Diarrhoea, Anaphylactic Reaction, Platelet Count Decreased, Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS
Dosage: 160mg/800mg daily, oral
Administration route: Oral
Indication: Ill-Defined Disorder
Start date: 2007-06-30
End date: 2007-07-14
Bactrim DS
Dosage: 160mg/800mg daily, oral
Administration route: Oral
Indication: Pneumocystis Jiroveci Pneumonia
Start date: 2007-06-30
End date: 2007-07-14
Fluconazole
Dosage: once daily, oral
Administration route: Oral
Start date: 2007-06-29
End date: 2007-07-14
Adverse event in 58 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a individual with unspecified qualification from United States on 2007-07-25
Patient: 58 year old male, weighing 88.1 kg (193.8 pounds)
Adverse reactions / side effects: Rash
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in 38 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a pharmacist from United States on 2007-07-24
Patient: 38 year old male
Adverse reactions / side effects: Angioedema
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Other drugs received by patient: Hydrochlorothiazide
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-07-23
Patient: male, weighing 71.7 kg (157.8 pounds)
Adverse reactions / side effects: Normochromic Normocytic Anaemia, Renal Failure Acute, Gastritis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Atripla
Administration route: Oral
Indication: HIV Infection
Start date: 2007-05-02
End date: 2007-05-16
Bactrim DS
Administration route: Oral
Indication: Antifungal Prophylaxis
Start date: 2007-05-02
End date: 2007-05-16
Ibuprofen
Administration route: Oral
Indication: Arthralgia
Start date: 2007-04-16
End date: 2007-05-16
Other drugs received by patient: Kaletra; Fluconazole; Zofran; Azithromycin
Adverse event in female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a individual with unspecified qualification from United States on 2007-07-09
Patient: female, weighing 104.0 kg (228.8 pounds)
Adverse reactions / side effects: Meniscus Lesion, Osteoarthritis, Hypotension, Atrial Fibrillation
Adverse event resulted in: hospitalization
Suspect drug(s):
Mercaptopurine
Dosage: 4620 mg
End date: 2007-06-18
Methotrexate
Dosage: 7305 mg
End date: 2007-06-14
Vincristine Sulfate
Dosage: 6 mg
End date: 2007-06-12
Allopurinol
Dosage: 12900mg
End date: 2007-06-26
Bactrim DS
Dosage: 1500 mg
End date: 2007-06-25
Leucovorin Calcium
Dosage: 465 mg
End date: 2007-06-16
Adverse event in 37 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a individual with unspecified qualification from United States on 2007-07-05
Patient: 37 year old male
Adverse reactions / side effects: Blood Bilirubin Increased, Anaemia, Alanine Aminotransferase Increased, Drug Hypersensitivity, Orthostatic Hypotension, Liver Disorder, Hepatomegaly, Aspartate Aminotransferase Increased, Haemolytic Anaemia, Meningitis Aseptic
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in 64 year old male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a pharmacist from United States on 2007-07-02
Patient: 64 year old male
Adverse reactions / side effects: Thrombocytopenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in male receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a individual with unspecified qualification from United States on 2007-06-29
Patient: male
Adverse reactions / side effects: Blood Bilirubin Increased, Alanine Aminotransferase Increased, Drug Hypersensitivity, Orthostatic Hypotension, Liver Disorder, Hepatomegaly, Aspartate Aminotransferase Increased, Haemolytic Anaemia, Meningitis Aseptic
Adverse event resulted in: hospitalization
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Adverse event in 47 year old female receiving Bactrim DS (Sulfamethoxazole / Trimethoprim)
Reported by a physician from United States on 2007-06-27
Patient: 47 year old female
Adverse reactions / side effects: Weight Decreased, Pruritus, Alanine Aminotransferase Increased, Cholestasis, Chromaturia, Liver Disorder, Hepatic Enzyme Increased, Abdominal Discomfort, Fatigue, Aspartate Aminotransferase Increased
Suspect drug(s):
Bactrim DS (Sulfamethoxazole / Trimethoprim)
Other drugs received by patient: Calcium Chloride; Ascorbic Acid
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