Nitrofurantoin (Nitrofurantoin) - Adverse Event Reports - Serious Event - Nausea

Adverse event in 34 year old female receiving Nitrofurantoin

Reported by a consumer/non-health professional from United States on 2007-07-11

Patient: 34 year old female, weighing 59.0 kg (129.7 pounds)

Adverse reactions / side effects: Vomiting, Nausea, Drug Hypersensitivity, Urticaria, Swollen Tongue, Hyperhidrosis, Hyperventilation, Auricular Swelling, Oedema Peripheral

Adverse event resulted in: hospitalization

Suspect drug(s):
Nitrofurantoin

Adverse event in 47 year old female receiving Nitrofurantoin

Reported by a physician from United States on 2007-05-10

Patient: 47 year old female, weighing 83.9 kg (184.6 pounds)

Adverse reactions / side effects: Blood Bilirubin Increased, Blood Bilirubin Unconjugated Increased, Chills, Pain, Urticaria, Headache, Constipation, Fatigue, Oedema, Blood Alkaline Phosphatase Increased, Nausea, Hepatitis Acute, Haemorrhoids, Drug Hypersensitivity, Alanine Aminotransferase Increased, Jaundice Cholestatic, Eosinophil Count Increased, Discomfort, Hepatic Enzyme Increased, Tremor, Faeces Pale, Flushing, Aspartate Aminotransferase Increased, Urine Colour Abnormal, Ocular Icterus, Bilirubin Conjugated Increased, Influenza Like Illness

Suspect drug(s):
Nitrofurantoin
    Dosage: 100 mg, oral
    Administration route: Oral
    Indication: Cystitis
    Start date: 2006-08-11
    End date: 2006-08-13

Estradiol
    Dosage: 0.05 mg, qd, transdermal
    Indication: Oestrogen Replacement Therapy
    Start date: 2006-07-01
    End date: 2006-08-01

Adverse event in 28 year old female receiving Nitrofurantoin

Reported by a individual with unspecified qualification from United Kingdom on 2007-04-16

Patient: 28 year old female

Adverse reactions / side effects: Vomiting, Malaise, Drug Exposure During Pregnancy, Nausea, Headache, Abortion Spontaneous

Adverse event resulted in: hospitalization

Suspect drug(s):
Nitrofurantoin