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Index of reports
> Cases resulting in other serious reactions (12)
Below is the selection of adverse event reports related to Omnicef (Cefdinir) that includes cases resulting in other serious reactions.
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 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 2007-04-13
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 2007-03-13
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 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 male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-03-05
Patient: male, weighing 48.1 kg (105.9 pounds)
Adverse reactions / side effects: Nephritis Interstitial
Suspect drug(s):
Omnicef (Cefdinir)
Adverse event in female receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-03-05
Patient: female, weighing 57.2 kg (125.8 pounds)
Adverse reactions / side effects: Choking Sensation, Nausea, Oedema Peripheral, Chest Pain, Rash, Panic Reaction
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Esomeprazole Magnesium; Ortho Evra; Factive; Respaire-SR-120
Adverse event in 57 year old female receiving Omnicef (Cefdinir)
Reported by a individual with unspecified qualification from United States on 2007-02-26
Patient: 57 year old female, weighing 74.8 kg (164.7 pounds)
Adverse reactions / side effects: Middle Insomnia, Pain in Extremity, Arthralgia, Pain, Hypoaesthesia, Crying
Suspect drug(s):
Omnicef (Cefdinir)
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-02-08
Patient: male, weighing 15.5 kg (34.1 pounds)
Adverse reactions / side effects: Confusional State, Psychomotor Hyperactivity, Excoriation, Abnormal Behaviour, Mental Status Changes, Fall, Repetitive Speech, Respiratory Tract Congestion, Incoherent, Poor Quality Sleep, Mania, Skin Papilloma, Upper Respiratory Tract Infection, Otitis Media, Disturbance in Attention, Cough
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Paracetamol; Pediatric Cough and Cold (Otc); Dtap Vaccine; M-M-R II; Poliovirus IPV Booster
Adverse event in male receiving Omnicef (Cefdinir)
Reported by a physician from United States on 2007-01-24
Patient: male, weighing 15.5 kg (34.1 pounds)
Adverse reactions / side effects: Confusional State, Psychomotor Hyperactivity, Abnormal Behaviour, Mental Status Changes, Repetitive Speech, Incoherent, Mania, Poor Quality Sleep, Disturbance in Attention
Suspect drug(s):
Omnicef (Cefdinir)
Other drugs received by patient: Paracetamol; Pediatric Cough and Cold (Otc)
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):
Azithromycin
Dosage: 250 mg, 2 tabs x1 then 1 tab daily oral
Administration route: Oral
Indication: Sinusitis
Omnicef
Dosage: 300 mg, 2 x day x 1 then daily oral
Administration route: Oral
Indication: Sinusitis
Other drugs received by patient: Lunesta; Amitriptyline HCL
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