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Prilosec (Omeprazole) - Adverse Event Reports - All Cases - Nausea

 



Index of reports > All cases (66) > Cases with Nausea (10)

Below is the selection of adverse event reports related to Prilosec (Omeprazole) that includes all cases where reactions include nausea.

Adverse event in 52 year old female receiving Prilosec (Omeprazole)

Reported by a consumer/non-health professional from United States on 2007-10-31

Patient: 52 year old female, weighing 81.6 kg (179.6 pounds)

Adverse reactions / side effects: Drug Effect Decreased, Glycosylated Haemoglobin Increased, Nausea, Stomach Discomfort, Abdominal Distension, Blood Glucose Increased

Suspect drug(s):
Symlin
    Dosage: 120, 60, 18 mcg;tid;sc
    Indication: Type 2 Diabetes Mellitus
    End date: 2006-01-01

Symlin
    Dosage: 120, 60, 18 mcg;tid;sc
    Indication: Type 2 Diabetes Mellitus
    Start date: 2006-01-01
    End date: 2006-05-01

Symlin
    Dosage: 120, 60, 18 mcg;tid;sc
    Indication: Type 2 Diabetes Mellitus
    Start date: 2006-05-01

Prilosec

Other drugs received by patient: Lantus; Humalog; Nexium; Prilosec



Adverse event in 81 year old female receiving Prilosec (Omeprazole)

Reported by a consumer/non-health professional from United States on 2007-10-23

Patient: 81 year old female, weighing 54.9 kg (120.7 pounds)

Adverse reactions / side effects: Vomiting, Diarrhoea, Nausea, Headache, Hyperhidrosis, Abdominal Pain Upper

Suspect drug(s):
Prilosec (Omeprazole)



Adverse event in 82 year old male receiving Prilosec (Omeprazole)

Reported by a physician from United States on 2007-10-18

Patient: 82 year old male, weighing 70.0 kg (154.0 pounds)

Adverse reactions / side effects: Tubulointerstitial Nephritis, Nausea, Anorexia, Renal Failure Acute

Adverse event resulted in: disablity

Suspect drug(s):
Prilosec
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-03-27
    End date: 2007-08-24

Prilosec
    Administration route: Oral
    Indication: Cough
    Start date: 2007-03-27
    End date: 2007-08-24

Aleve
    Start date: 2007-08-01

Other drugs received by patient: Prednisone; Prevacid; Doxazosin Mesylate; Lexapro; Lexapro; Avapro; Sonata; Alprazolam; Alprazolam



Adverse event in 37 year old male receiving Prilosec (Omeprazole)

Reported by a physician from United States on 2007-06-22

Patient: 37 year old male

Adverse reactions / side effects: Chest Discomfort, Nausea, Alanine Aminotransferase Increased, Coronary Artery Disease, Hyperhidrosis, Malaise, Fatigue, Palpitations, Chest Pain, Dizziness, Asthenia, Hypertension

Adverse event resulted in: hospitalization

Suspect drug(s):
Zocor
    Administration route: Oral
    Start date: 2001-04-01
    End date: 2001-05-01

Toprol-XL

Prilosec

Pravachol



Adverse event in 86 year old female receiving Prilosec (Omeprazole)

Reported by a consumer/non-health professional from United States on 2007-06-05

Patient: 86 year old female

Adverse reactions / side effects: Nausea, Sneezing

Suspect drug(s):
Prilosec (Omeprazole)

Other drugs received by patient: Coumadin; Furosemide; Toprol-XL; Digitex; Potassium Chloride



Adverse event in female receiving Prilosec (Omeprazole)

Reported by a consumer/non-health professional from United States on 2007-06-05

Patient: female, weighing 63.5 kg (139.7 pounds)

Adverse reactions / side effects: Dysgeusia, Nausea, Abdominal Distension, Pharmaceutical Product Complaint

Suspect drug(s):
Prilosec (Omeprazole)

Other drugs received by patient: Lipitor



Adverse event in female receiving Prilosec (Omeprazole)

Reported by a consumer/non-health professional from United States on 2007-06-01

Patient: female

Adverse reactions / side effects: Malabsorption, Muscle Atrophy, Pneumonia, Psychomotor Hyperactivity, Drug Ineffective, Nausea, Crohn's Disease, Anxiety, Fatigue, Insomnia, Bone Disorder, Gastrooesophageal Reflux Disease

Adverse event resulted in: hospitalization

Suspect drug(s):
Prednisone TAB
    Indication: Crohn's Disease

Chantix
    Indication: EX-Smoker

Zithromax
    Indication: Pneumonia
    Start date: 2007-01-01
    End date: 2007-01-01

Amoxicillin
    Indication: Pneumonia

Drug, Unspecified

Prevacid
    Indication: Gastrooesophageal Reflux Disease

Prilosec
    Indication: Gastrooesophageal Reflux Disease

Acetylsalicylic Acid SRT
    Indication: Cardiovascular Event Prophylaxis

Other drugs received by patient: Drug, Unspecified; Asacol; Prilosec; Acetylsalicylic Acid SRT



Adverse event in female receiving Prilosec (Omeprazole)

Reported by a consumer/non-health professional from United States on 2007-05-18

Patient: female

Adverse reactions / side effects: Malabsorption, Muscle Atrophy, Pneumonia, Psychomotor Hyperactivity, Drug Ineffective, Nausea, Crohn's Disease, Anxiety, Fatigue, Insomnia, Bone Disorder, Gastrooesophageal Reflux Disease

Adverse event resulted in: hospitalization

Suspect drug(s):
Prednisone TAB
    Indication: Crohn's Disease

Chantix
    Indication: EX-Smoker

Zithromax
    Indication: Pneumonia
    Start date: 2007-01-01
    End date: 2007-01-01

Amoxicillin
    Indication: Pneumonia

Drug, Unspecified

Prevacid
    Indication: Gastrooesophageal Reflux Disease

Prilosec
    Indication: Gastrooesophageal Reflux Disease

Acetylsalicylic Acid SRT
    Indication: Cardiovascular Event Prophylaxis

Other drugs received by patient: Drug, Unspecified; Asacol



Adverse event in female receiving Prilosec (Omeprazole)

Reported by a lawyer from United States on 2007-02-14

Patient: female, weighing 85.7 kg (188.5 pounds)

Adverse reactions / side effects: Agitation, Abdominal Pain, Pruritus, Sciatica, Headache, Erythema, Delusion, Duodenitis, Oesophagitis, Uterine Leiomyoma, Blood Pressure Inadequately Controlled, Pneumonitis, Back Pain, Chest Discomfort, Hiatus Hernia, Pain in Extremity, Hyperglycaemia, Coronary Artery Disease, Hypoaesthesia, Dehydration, Disorientation, Myalgia, Chest Pain, Dizziness, Intestinal Polyp, Vomiting, Viral Infection, Nausea, Musculoskeletal Pain, Rash, Purpura, Facial Pain, Hypertensive Crisis, Limb Discomfort, Diarrhoea, Arthralgia, Pollakiuria, Gastroenteritis, Bronchitis, Infection

Adverse event resulted in: hospitalization

Suspect drug(s):
Procardia XL
    Administration route: Oral
    Indication: Hypertension

Procardia XL
    Administration route: Oral
    Start date: 2001-01-22
    End date: 2001-02-04

Procardia XL
    Administration route: Oral
    Start date: 2001-02-05
    End date: 2003-08-29

Nifedipine
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-02-01
    End date: 2004-01-01

Vasotec
    Start date: 1998-12-13
    End date: 1999-03-20

Cozaar
    Administration route: Oral
    Start date: 1999-12-07
    End date: 2001-01-22

Hyzaar
    Start date: 1999-12-07
    End date: 2000-01-01

Toprol-XL
    Start date: 1999-03-20

Paxil
    Start date: 1999-03-20

Clonidine
    Start date: 1999-03-20

Biaxin

Prilosec
    Start date: 2001-12-04
    End date: 2003-01-01

Premarin
    Start date: 2002-02-25

Diovane
    Start date: 2002-02-25
    End date: 2002-05-06

Benicar
    End date: 2003-08-29

Catapres
    Start date: 2001-01-22
    End date: 2001-01-01

Oxycodone
    Indication: Pain
    Start date: 2001-02-05

Lopressor
    Start date: 2001-01-01

Protonix
    Start date: 2001-01-01

Adalat
    Start date: 2001-02-05

Prevacid
    Start date: 2000-01-10

Nitrol
    Start date: 2002-05-06

Heparin
    Start date: 2002-05-06

Aspirin
    Start date: 2002-05-06

Vicodin ES



Adverse event in female receiving Prilosec (Omeprazole)

Reported by a lawyer from United States on 2007-01-31

Patient: female, weighing 85.7 kg (188.5 pounds)

Adverse reactions / side effects: Abdominal Pain, Pruritus, Sciatica, Urticaria, Erythema, Delusion, Duodenitis, Oesophagitis, Uterine Leiomyoma, Blood Pressure Inadequately Controlled, Pneumonitis, Back Pain, Chest Discomfort, Hiatus Hernia, Pain in Extremity, Hyperglycaemia, Coronary Artery Disease, Hypoaesthesia, Dehydration, Chest Pain, Dizziness, Intestinal Polyp, Viral Infection, Vomiting, Nausea, Musculoskeletal Pain, Purpura, Facial Pain, Hypertensive Crisis, Limb Discomfort, Diarrhoea, Arthralgia, Gastroenteritis, Bronchitis

Adverse event resulted in: hospitalization

Suspect drug(s):
Procardia XL
    Administration route: Oral
    Indication: Hypertension

Procardia XL
    Administration route: Oral
    Start date: 2001-01-22
    End date: 2001-02-04

Procardia XL
    Administration route: Oral
    Start date: 2001-02-05
    End date: 2003-08-29

Nifedipine
    Administration route: Oral
    Indication: Hypertension
    Start date: 2004-02-01
    End date: 2004-01-01

Vasotec
    Start date: 1998-12-13
    End date: 1999-03-20

Cozaar
    Administration route: Oral
    Start date: 1999-12-07
    End date: 2001-01-22

Hyzaar
    Start date: 1999-12-07
    End date: 2000-01-01

Toprol-XL
    Start date: 1999-03-20

Paxil
    Start date: 1999-03-20

Clonidine
    Start date: 1999-03-20

Biaxin

Prilosec
    Start date: 2001-12-04
    End date: 2003-01-01

Premarin
    Start date: 2002-02-25

Diovane
    Start date: 2002-02-25
    End date: 2002-05-06

Benicar
    End date: 2003-08-29

Catapres
    Start date: 2001-01-22
    End date: 2001-01-01

Oxycodone HCL
    Indication: Pain
    Start date: 2001-02-05

Lopressor
    Start date: 2001-01-01

Protonix
    Start date: 2001-01-01

Adalat
    Start date: 2001-02-05

Prevacid
    Start date: 2000-01-10

Nitrol
    Start date: 2002-05-06

Heparin
    Start date: 2002-05-06

Aspirin
    Start date: 2002-05-06

Vicodin ES

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