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Macrobid (Nitrofurantoin) - Life Threatening Events - Suspected Cause - Side Effect Reports

 
 



Index of reports > Life Threatening Events (11)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Macrobid (Nitrofurantoin) life threatening events. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Macrobid side effects in 57 year old female

Reported by a individual with unspecified qualification from United States on 2012-06-20

Patient: 57 year old female, weighing 144.2 kg (317.3 pounds)

Reactions: Malaise, Activities of Daily Living Impaired, Yellow Skin, Impaired Work Ability, Ocular Icterus, Asthenia

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Macrobid



Possible Macrobid side effects in 83 year old female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-06-15

Patient: 83 year old female

Reactions: Oedema Peripheral, Oedema, Erythema, Skin Warm, Tremor

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Macrobid



Possible Macrobid side effects in 41 year old female

Reported by a consumer/non-health professional from United States on 2012-02-29

Patient: 41 year old female, weighing 81.6 kg (179.6 pounds)

Reactions: Chest Discomfort, Tongue Discolouration, Dyspnoea, Nausea, Headache, Hypoaesthesia, Paraesthesia, Upper Respiratory Tract Infection, Diarrhoea, Chest Pain, Dizziness, Asthenia

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Macrobid



Possible Macrobid side effects in female

Reported by a physician from Ireland on 2012-02-08

Patient: female

Reactions: Blood Bilirubin Increased, Jaundice, Blood Alkaline Phosphatase Increased, Body Temperature Increased, Alanine Aminotransferase Increased, Urinary Tract Infection, Chromaturia, C-Reactive Protein Increased, Gamma-Glutamyltransferase Increased, RED Blood Cell Sedimentation Rate Increased

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Valdoxan
    Administration route: Oral
    Indication: Depression
    Start date: 2011-02-14
    End date: 2011-03-01

Clarithromycin
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-05-25
    End date: 2011-06-03

Lamictal
    Administration route: Oral
    Indication: Depression
    Start date: 2011-05-24

Lamictal
    Dosage: 200mg daily
    End date: 2011-06-08

Augmentin '125'
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-05-25
    End date: 2011-06-01

Valdoxan
    Administration route: Oral
    Start date: 2011-03-01
    End date: 2011-06-08

Agomelatin
    Dosage: 50 mg daily
    End date: 2011-06-08

Agomelatin
    Administration route: Oral
    Indication: Depression
    Start date: 2011-02-14

Macrobid
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-05-26
    End date: 2011-06-03

Other drugs received by patient: Madopar; Mirtazapine; Memantine Hydrochloride; Plavix



Possible Macrobid side effects in 57 year old female

Reported by a consumer/non-health professional from United States on 2012-01-23

Patient: 57 year old female, weighing 63.5 kg (139.7 pounds)

Reactions: Abdominal Pain, Nausea, Headache, Myalgia, Impaired Driving Ability, Skin Discolouration, Arthralgia, Influenza

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Macrobid



Possible Macrobid side effects in female

Reported by a physician from Ireland on 2011-10-25

Patient: female

Reactions: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Jaundice, Body Temperature Increased, Urinary Tract Infection, Alanine Aminotransferase Increased, Chromaturia, Gamma-Glutamyltransferase Increased

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Clarithromycin
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-05-25
    End date: 2011-06-03

Macrobid
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-05-26
    End date: 2011-06-03

Agomelatin
    Dosage: 50 mg daily
    End date: 2011-06-08

Augmentin
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-06-07

Lamictal
    Administration route: Oral
    Indication: Depression
    Start date: 2011-05-24

Agomelatin
    Administration route: Oral
    Indication: Depression
    Start date: 2011-02-14

Lamictal
    Dosage: 200mg daily
    End date: 2011-06-08

Other drugs received by patient: Plavix; Memantine Hydrochloride; Mirtazapine; Madopar



Possible Macrobid side effects in 85 year old male

Reported by a individual with unspecified qualification from United States on 2011-10-24

Patient: 85 year old male

Reactions: Chills, Pyrexia, Fatigue, Cyanosis, Oedema Peripheral, Contraindication To Medical Treatment, Cough, Dyspnoea, Chest Discomfort, Pain in Extremity, Muscular Weakness, Arthralgia, Joint Swelling, Butterfly Rash, Asthenia, Feeling Abnormal

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Macrobid



Possible Macrobid side effects in 52 year old female

Reported by a individual with unspecified qualification from Canada on 2011-10-20

Patient: 52 year old female

Reactions: Crohn's Disease, Hypotension, Drug Hypersensitivity, Anaphylactic Shock, Drug Interaction, Cystitis, Disease Progression, Abdominal Discomfort, Dehydration, Abdominal Distension, Dizziness, Incision Site Abscess, Bladder Operation

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Macrobid
    Indication: Product Used FOR Unknown Indication

Codeine Sulfate
    Indication: Product Used FOR Unknown Indication

Avelox
    Indication: Product Used FOR Unknown Indication

Remicade
    Dosage: 1 every 8 week(s)

Amoxicillin
    Indication: Product Used FOR Unknown Indication

Remicade
    Dosage: 1 every 8 week(s)
    Indication: Product Used FOR Unknown Indication

Remicade
    Dosage: 1 every 8 week(s)

Remicade
    Dosage: 1 every 8 week(s)



Possible Macrobid side effects in 84 year old female

Reported by a individual with unspecified qualification from Canada on 2011-10-19

Patient: 84 year old female, weighing 55.8 kg (122.7 pounds)

Reactions: Dyspnoea, Chest Discomfort, Chills, Tremor, Fatigue, Arthralgia, Ocular Hyperaemia, Ear Pain, Asthenia, Oxygen Saturation Decreased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Macrobid

Other drugs received by patient: Hydrochlorothiazide; Hytrin



Possible Macrobid side effects in 60 year old female

Reported by a individual with unspecified qualification from Canada on 2011-10-19

Patient: 60 year old female, weighing 71.2 kg (156.7 pounds)

Reactions: Abdominal Pain, Goitre, Chills, Urticaria, Hyperhidrosis, Pallor, Autoimmune Thyroiditis, Abdominal Discomfort, Weight Increased, Pruritus Generalised, Malaise, Fatigue, Cyanosis, Oedema Peripheral, Blood Pressure Increased, Respiratory Rate Increased, Aphagia, Dyspnoea, Stomatitis, Vomiting, Nausea, Drug Hypersensitivity, Tremor, Flushing, Diarrhoea, Dehydration, Heart Rate Increased, Thyroid Disorder

Adverse event resulted in: life threatening event

Drug(s) suspected as cause:
Macrobid

Other drugs received by patient: Diovan; Acebutolol; Vitamin D



Possible Macrobid side effects in 83 year old female

Reported by a individual with unspecified qualification from Canada on 2011-10-18

Patient: 83 year old female

Reactions: Oedema Peripheral, Oedema, Erythema, Skin Warm, Tremor

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Macrobid

Other drugs received by patient: Benadryl; Noroxin

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