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Index of reports
> Cases resulting in disability (3)
Below is the selection of adverse event reports related to Omnicef (Cefdinir) that includes cases resulting in disability.
Adverse event in 47 year old receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-06-14
Patient: 47 year old
Adverse reactions / side effects: Anxiety, Nerve Injury, Psychomotor Skills Impaired, Fear
Adverse event resulted in: disablity
Suspect drug(s):
Omnicef (Cefdinir)
Adverse event in 55 year old male receiving Omnicef (Cefdinir)
Reported by a consumer/non-health professional from United States on 2007-06-14
Patient: 55 year old male
Adverse reactions / side effects: Diabetes Mellitus, Skin Lesion, Vasculitis, Rash, Arthritis, Infection
Adverse event resulted in: life threatening event, disablity
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
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