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Index of reports
> All cases (31)
> Cases with Diarrhoea (8)
Below is the selection of adverse event reports related to Omnicef (Cefdinir) that includes all cases where reactions include diarrhoea.
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-06-15
Patient: male
Adverse reactions / side effects: Diarrhoea, Gastroenteritis Rotavirus, Dehydration, Colitis, Clostridial Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Indication: Otitis Media
Start date: 2007-02-19
End date: 2007-02-21
Augmentin '125'
Indication: Otitis Media
Start date: 2007-02-17
End date: 2007-02-19
Adverse event in 57 year old female receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional on 2007-06-14
Patient: 57 year old female
Adverse reactions / side effects: Rheumatoid Arthritis, Movement Disorder, Joint Swelling, Diarrhoea, Haemorrhage, Oedema Peripheral, Pain
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Adverse event in 2 year old male receiving Omnicef (Cefdinir)
Reported by a individual with unspecified qualification from United States on 2007-04-19
Patient: 2 year old male, weighing 12.2 kg (26.9 pounds)
Adverse reactions / side effects: Irritability, Vomiting, Diarrhoea, Anorexia, Thirst, Crying
Suspect drug(s):
Omnicef
Dosage: 3.75ml 1xday po
Administration route: Oral
Indication: Sinusitis
Start date: 2007-04-14
End date: 2007-04-15
Omnicef
Dosage: 3.75ml 1xday po
Administration route: Oral
Indication: Sinusitis
Start date: 2007-04-17
End date: 2007-04-17
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-03-28
Patient: female
Adverse reactions / side effects: Vomiting, Pain in Extremity, Pain, Mucous Stools, Pyrexia, Overgrowth Bacterial, Haematochezia, Diarrhoea, Gastroenteritis, Influenza
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Otitis Media
Start date: 2005-11-01
Omnicef
Administration route: Oral
Start date: 2007-02-15
Adverse event in 42 year old female receiving Omnicef (Cefdinir)
Reported by a individual with unspecified qualification from United States on 2007-03-09
Patient: 42 year old female, weighing 76.2 kg (167.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Diarrhoea, Abdominal Distension, Vaginal Pain
Suspect drug(s):
Omnicef (Cefdinir)
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-03-01
Patient: female
Adverse reactions / side effects: Haematochezia, Vomiting, Diarrhoea, Pain in Extremity, Pain, Pyrexia, Overgrowth Bacterial
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2005-11-01
Omnicef
Administration route: Oral
Indication: Ear Infection
Start date: 2007-02-15
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-02-07
Patient: female
Adverse reactions / side effects: Photosensitivity Reaction, Skin Exfoliation, Extrasystoles, Tonsillitis, House Dust Allergy, Weight Increased, Food Allergy, Intervertebral Disc Protrusion, White Blood Cell Count Decreased, Stomatitis, Drug Hypersensitivity, Allergy TO Chemicals, Milk Allergy, Blood Glucose Decreased, Diarrhoea, Swelling, Vasculitis, Skin Nodule, Influenza Like Illness
Adverse event resulted in: hospitalization
Suspect drug(s):
Pegasys
Dosage: patient was on treatment for 9 months, 2 years ago.
Indication: Hepatitis C
Start date: 2005-06-15
Ribavirin
Dosage: patient was on treatment for 9 months, 2 years ago.
Indication: Drug USE FOR Unknown Indication
Start date: 2005-06-15
Omnicef
Indication: Tonsillitis
Other drugs received by patient: Vitamins NOS
Adverse event in 57 year old female receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-01-12
Patient: 57 year old female, weighing 66.7 kg (146.7 pounds)
Adverse reactions / side effects: Diarrhoea
Suspect drug(s):
Omnicef
Dosage: 300 mg, 2 x day x 1 then daily oral
Administration route: Oral
Indication: Sinusitis
Azithromycin
Dosage: 250 mg, 2 tabs x1 then 1 tab daily oral
Administration route: Oral
Indication: Sinusitis
Other drugs received by patient: Lunesta; Amitriptyline HCL
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