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Index of reports
> Cases resulting in hospitalization (16)
Below is the selection of adverse event reports related to Omnicef (Cefdinir) that includes cases resulting in hospitalization.
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-10-25
Patient: male, weighing 104.5 kg (229.9 pounds)
Adverse reactions / side effects: Fall, Polyneuropathy, Joint Stiffness, Abdominal Pain Upper, Myalgia, Neuropathy Peripheral, Balance Disorder, Skin Lesion, Chest Pain, Coordination Abnormal, Bronchiolitis, Blood Pressure Increased, Back Pain, Pain in Extremity, Muscular Weakness, Rash, Hypoaesthesia, Paraesthesia, Arthralgia, Bronchitis, Gait Disturbance, Hyporeflexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Lower Respiratory Tract Infection
Start date: 2006-02-03
End date: 2006-02-08
Omnicef
Indication: Cough
Omnicef
Indication: Upper Respiratory Tract Infection
Other drugs received by patient: Mucinex D; Benzonatate; Ropinirole HCL; Prednisone; Acetylsalicylic Acid SRT; Fluticasone Propionate
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-07-06
Patient: female, weighing 68.1 kg (149.8 pounds)
Adverse reactions / side effects: Anxiety, Neuropathy, Dyspnoea, Paranoia, Fear, Muscular Weakness
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Mesalazine; Valacyclovir HCL; Tizanidine HCL; Leflunomide; Zolpidem Tartrate; Panocaps; Meperidine HCL; Clonidine; Topiramate; Pantoprazole Sodium; Cetirizine Hydrochloride; Fluticasone Propionate
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):
Augmentin '125'
Indication: Otitis Media
Start date: 2007-02-17
End date: 2007-02-19
Omnicef
Indication: Otitis Media
Start date: 2007-02-19
End date: 2007-02-21
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 36 year old male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-06-08
Patient: 36 year old male
Adverse reactions / side effects: LIP Swelling, Oral Mucosal Blistering, Rash Pruritic, Oedema Peripheral, Blindness, Conjunctival Scar, Pharyngitis, Stevens-Johnson Syndrome
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Lamictal
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-10-23
End date: 2006-11-21
Medrol
Omnicef
Indication: Pharyngitis
Vicodin
Zithromax
Other drugs received by patient: Sertraline Hydrochloride; Mometasone Furoate; Sumatriptan Succinate; Hydrochlorothiazide
Adverse event in 9 month old female receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-05-01
Patient: 9 month old female, weighing 8.6 kg (19.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Intussusception, Diarrhoea Haemorrhagic, Lethargy
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-04-25
Patient: male, weighing 25.0 kg (54.9 pounds)
Adverse reactions / side effects: Henoch-Schonlein Purpura, Joint Swelling, Adverse Drug Reaction, Pain, Serum Sickness, Rash Maculo-Papular
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Nasal Congestion
Start date: 2006-12-22
End date: 2006-12-31
Omnicef
Indication: Ear Tube Insertion
Omnicef
Indication: Sputum Discoloured
Omnicef
Indication: Pyrexia
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-04-13
Patient: female, weighing 61.3 kg (134.8 pounds)
Adverse reactions / side effects: Grand MAL Convulsion, Muscle Twitching, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Mefloquine; Mefloquine; Mefloquine; Mefloquine; Mefloquine; Mefloquine; Anagrelide HCL; Anagrelide HCL
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-04-05
Patient: male, weighing 15.9 kg (35.0 pounds)
Adverse reactions / side effects: Body Temperature Decreased
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Sinusitis
Start date: 2007-02-08
End date: 2007-02-28
Omnicef
Administration route: Oral
Start date: 2007-03-26
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-03-13
Patient: male, weighing 79.5 kg (174.8 pounds)
Adverse reactions / side effects: Pneumonia, Drug Ineffective
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Levofloxacin; Mucinex DM
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-03-13
Patient: male, weighing 104.5 kg (229.9 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Pain in Extremity, Rash, Polyneuropathy, Abdominal Pain Upper, Paraesthesia, Myalgia, Arthralgia, Skin Lesion, Chest Pain, Gait Disturbance, Coordination Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Lower Respiratory Tract Infection
Start date: 2006-02-03
End date: 2006-02-08
Omnicef
Indication: Cough
Omnicef
Indication: Upper Respiratory Tract Infection
Other drugs received by patient: Mucinex; Benzonatate; Ropinirole HCL; Prednisone
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-03-07
Patient: male, weighing 25.0 kg (54.9 pounds)
Adverse reactions / side effects: Henoch-Schonlein Purpura, Joint Swelling, Adverse Drug Reaction, Pain, Serum Sickness, Rash Maculo-Papular
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef
Administration route: Oral
Indication: Ear Congestion
Start date: 2006-12-20
End date: 2007-01-02
Omnicef
Indication: Ear Tube Insertion
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 male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-02-16
Patient: male, weighing 81.7 kg (179.8 pounds)
Adverse reactions / side effects: Hepatomegaly, Dehydration, Abdominal Distension, Helicobacter Infection, Gastric Ulcer, Asthenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Pantoprazole Sodium; Metoprolol Succinate; Phenergan; Digoxin
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):
Omnicef
Indication: Tonsillitis
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
Other drugs received by patient: Vitamins NOS
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a pharmacist from United States on 2007-01-25
Patient: female, weighing 67.1 kg (147.7 pounds)
Adverse reactions / side effects: Chest Pain, Headache
Adverse event resulted in: hospitalization
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Hydrocodone Syrup
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