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Omnicef (Cefdinir) - Adverse Event Reports - Serious Event - Pain

 



Index of reports > Cases resulting in a serious event (27) > Cases with Pain (5)

Below is the selection of adverse event reports related to Omnicef (Cefdinir) that includes cases resulting in a serious event where reactions include pain.

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 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 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 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)

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