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Index of reports
> All cases (77)
Below is the selection of adverse event reports related to Bactrim DS (Sulfamethoxazole / Trimethoprim) that includes all cases.
Reports 1 - 25 of 77 Next >>
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 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 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 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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