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Omnicef (Cefdinir) - Adverse Event Reports - All Cases - Pain

 



Index of reports > All cases (31) > Cases with Pain (6)

Below is the selection of adverse event reports related to Omnicef (Cefdinir) that includes all cases 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 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 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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