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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Duricef (Cefadroxil). 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 all available reports.
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 (9)
Cases resulting in a serious event (9)
Cases resulting in life threatening events (2)
Cases resulting in hospitalization (5)
Cases resulting in other serious reactions (4)
Adverse event in 51 year old male receiving Duricef (Cefadroxil)
Reported by a individual with unspecified qualification from Indonesia on 2007-10-12
Patient: 51 year old male
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Hepatic Function Abnormal, Alanine Aminotransferase Increased, Protein Total Decreased, Wound Infection Staphylococcal, Drug Rash With Eosinophilia and Systemic Symptoms, Myalgia, Renal Impairment, Postoperative Wound Infection, Arthralgia, Aspartate Aminotransferase Increased, Lymphocyte Morphology Abnormal, Dermatitis Exfoliative
Adverse event resulted in: hospitalization
Suspect drug(s):
Duricef (Cefadroxil)
Adverse event in male receiving Duricef (Cefadroxil)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-09
Patient: male
Adverse reactions / side effects: Nausea, Diarrhoea, Drug Ineffective, Sepsis, Rectal Abscess
Suspect drug(s):
Duricef (Cefadroxil)
Other drugs received by patient: Toprol-XL; Finasteride; Ambien; Percocet; Xanax; Ativan; Glucosamine W / Methylsulfonylmethane
Adverse event in 9 year old male receiving Duricef (Cefadroxil)
Reported by a physician from France on 2007-06-20
Patient: 9 year old male
Adverse reactions / side effects: Eyelid Oedema, LIP Swelling, Face Oedema, Stomatitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Duricef
Dosage: oral
Administration route: Oral
Indication: Tonsillitis
Start date: 2007-05-02
End date: 2007-05-07
Surgam (Tiaprofenac Acid)
Dosage: oral
Administration route: Oral
Indication: Tonsillitis
Start date: 2007-05-02
End date: 2007-05-07
Adverse event in 41 year old female receiving Duricef (Cefadroxil)
Reported by a health professional (non-physician/pharmacist) from France on 2007-05-03
Patient: 41 year old female
Adverse reactions / side effects: Cytolytic Hepatitis, Stevens-Johnson Syndrome, Eosinophilia
Adverse event resulted in: hospitalization
Suspect drug(s):
Duricef
Dosage: 1 g, bid, oral
Administration route: Oral
Indication: Tonsillitis
Start date: 1996-08-07
End date: 1996-08-09
Claradol / 00020001 (Paracetamol) 1G
Dosage: 1 g, tid, oral
Administration route: Oral
Start date: 1996-08-07
End date: 1996-08-09
Ribatran (Chymotrypsin, Ribonuclease, Trypsin)
Dosage: 1 dose, tid, oral
Administration route: Oral
Start date: 1996-08-07
End date: 1996-08-09
Adverse event in 41 year old male receiving Duricef (Cefadroxil)
Reported by a physician from France on 2007-04-06
Patient: 41 year old male
Adverse reactions / side effects: Nausea, Anaphylactic Shock
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Duricef (Cefadroxil)
Adverse event in 40 year old female receiving Duricef (Cefadroxil)
Reported by a physician from France on 2007-03-13
Patient: 40 year old female
Adverse reactions / side effects: Pruritus Generalised, Type IV Hypersensitivity Reaction, Purpura, Epistaxis
Suspect drug(s):
Duricef (Cefadroxil)
Adverse event in 59 year old female receiving Duricef (Cefadroxil)
Reported by a individual with unspecified qualification from Estonia on 2007-02-22
Patient: 59 year old female
Adverse reactions / side effects: Angioedema, Dyspnoea, Tongue Oedema, Pyrexia, Local Swelling, Face Oedema, Oedema Mouth, Urinary Retention, Feeling Abnormal
Suspect drug(s):
Duricef (Cefadroxil)
Adverse event in male receiving Duricef (Cefadroxil)
Reported by a individual with unspecified qualification from United States on 2007-01-31
Patient: male, weighing 24.0 kg (52.9 pounds)
Adverse reactions / side effects: Vomiting, Dyspnoea, Medication Error, Chest Pain, Contraindication TO Medical Treatment, Epistaxis, Abdominal Pain Upper
Suspect drug(s):
Duricef (Cefadroxil)
Adverse event in 31 year old female receiving Duricef (Cefadroxil)
Reported by a individual with unspecified qualification from Sweden on 2007-01-29
Patient: 31 year old female
Adverse reactions / side effects: Flushing, Thrombosis, Toxic Epidermal Necrolysis, Eye Excision, Unevaluable Event, Eye Infection
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Duricef
Dosage: oral
Administration route: Oral
Indication: Nasopharyngeal Disorder
Start date: 2006-08-24
End date: 2006-08-26
Duricef
Dosage: oral
Administration route: Oral
Indication: Pharyngeal Oedema
Start date: 2006-08-24
End date: 2006-08-26
Duricef
Dosage: oral
Administration route: Oral
Indication: Pharyngolaryngeal Pain
Start date: 2006-08-24
End date: 2006-08-26
Ibuprofen
Dosage: oral
Administration route: Oral
Indication: Nasopharyngeal Disorder
Start date: 2006-08-24
End date: 2006-08-26
Ibuprofen
Dosage: oral
Administration route: Oral
Indication: Pharyngeal Oedema
Start date: 2006-08-24
End date: 2006-08-26
Ibuprofen
Dosage: oral
Administration route: Oral
Indication: Pharyngolaryngeal Pain
Start date: 2006-08-24
End date: 2006-08-26
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