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Motrin (Ibuprofen) - Adverse Event Reports - Other Serious Reactions - Fatigue

 



Index of reports > Cases resulting in other serious reactions (27) > Cases with Fatigue (4)

Below is the selection of adverse event reports related to Motrin (Ibuprofen) that includes cases resulting in other serious reactions where reactions include fatigue.

Adverse event in female receiving Motrin (Ibuprofen)

Reported by a consumer/non-health professional from United States on 2007-10-17

Patient: female, weighing 77.3 kg (170.0 pounds)

Adverse reactions / side effects: Nerve Injury, Drug Ineffective, Drug Interaction, Pelvic Pain, Somnolence, Suicidal Ideation, Thinking Abnormal, Fatigue, Chest Pain, Clumsiness, Hysterectomy, Panic Attack, Loss of Employment, Incision Site Infection, Limb Injury, Vision Blurred, Gait Disturbance, Depressed Mood

Adverse event resulted in: hospitalization

Suspect drug(s):
Gabapentin
    Indication: Pelvic Pain

Gabapentin
    Indication: Nerve Injury

Motrin
    Indication: Pelvic Pain

Other drugs received by patient possibly interacting with the suspect drug:
Xanax
    Indication: Psychomotor Hyperactivity

Xanax
    Indication: Depression

Hismanal

Other drugs received by patient: Lopressor; Mevacor; Claritin; Dyazide; Aspirin



Adverse event in female receiving Motrin (Ibuprofen)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-03-23

Patient: female, weighing 64.4 kg (141.7 pounds)

Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Flatulence, Gallbladder Disorder, Back Pain, Steatorrhoea, Pain in Extremity, Abnormal Faeces, Tremor, Fungal Infection, Breath Sounds Abnormal, Insomnia, Body Temperature Increased, Drug Ineffective, Drug Interaction, Tonsillitis, Somnolence, Constipation, Culture Stool Positive, Abdominal Pain Upper, Myalgia, Fatigue, Anorectal Disorder, Dizziness, Abdominal Distension, Depression, Gastrooesophageal Reflux Disease, Blood Pressure Increased, Vomiting, Nausea, Muscular Weakness, Visual Disturbance, Diarrhoea, Heart Rate Increased, Hypothyroidism, Salmonellosis, Feeling Drunk, Gravitational Oedema

Suspect drug(s):
Flagyl
    Indication: Prophylaxis

Vancomycin
    Administration route: Oral
    Indication: Ill-Defined Disorder

Motrin
    Dosage: daily dose:1200mg
    Indication: Pain

Other drugs received by patient possibly interacting with the suspect drug:
Vfend
    Indication: Candidiasis

Vfend

Ambien
    Dosage: text:unknown
    Indication: Insomnia
    Start date: 2006-01-01
    End date: 2006-02-27

Gabitril
    Indication: Insomnia

PEN-VEE K
    Administration route: Oral
    Indication: Ill-Defined Disorder

PEN-VEE K
    Administration route: Oral

Other drugs received by patient: Provigil; Nortriptyline HCL; Drospirenone + Ethinyl Estradiol; TPN; Acidophilus; Yasmin



Adverse event in 21 year old female receiving Motrin (Ibuprofen)

Reported by a physician from United States on 2007-02-05

Patient: 21 year old female

Adverse reactions / side effects: Abdominal Pain, Jaundice, Weight Decreased, Malaise, Fatigue, Pruritus, Self-Medication, Liver Disorder

Suspect drug(s):
Bextra
    Start date: 2004-12-01
    End date: 2004-12-01

Motrin
    Start date: 2004-12-01
    End date: 2004-12-01

Other drugs received by patient: Birth Control Pill; Multi-Vitamin; Atarax; Bactrim



Adverse event in 73 year old female receiving Motrin (Ibuprofen)

Reported by a physician from United States on 2007-01-19

Patient: 73 year old female

Adverse reactions / side effects: Gastrointestinal Haemorrhage, Pain, Dyspnoea Exertional, Haematocrit Decreased, Fatigue, Iron Deficiency Anaemia, Pulmonary Oedema, Muscle Spasms, Hiatus Hernia, Stomach Discomfort, Occult Blood Positive, Haemoglobin Decreased, Syncope, Diverticulum, Ventricular Tachycardia, Suicide Attempt, Asthenia, Depressed Mood

Adverse event resulted in: life threatening event, hospitalization

Suspect drug(s):
Aleve
    Dosage: total daily dose: 880 mg unit dose: 220 mg
    Administration route: Oral
    Indication: Arthralgia

Motrin
    Dosage: total daily dose: 2400 mg unit dose: 800 mg
    Indication: Osteoarthritis

Naprosyn
    Indication: Osteoarthritis

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