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Prevacid (Lansoprazole) - Adverse Event Reports - All Cases - Dizziness

 



Index of reports > All cases (45) > Cases with Dizziness (7)

Below is the selection of adverse event reports related to Prevacid (Lansoprazole) that includes all cases where reactions include dizziness.

Adverse event in 60 year old female receiving Prevacid (Lansoprazole)

Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-09

Patient: 60 year old female, weighing 77.3 kg (170.1 pounds)

Adverse reactions / side effects: Nausea, Dizziness, Vision Blurred, Nervousness

Suspect drug(s):
Prevacid
    Dosage: 30 mg, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-05-02
    End date: 2007-05-03

Pepcid Complete (Famotidine)
    Dosage: 1 tab, 1 in 1 d, per oral
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2007-05-02

Other drugs received by patient: Celebrex; Flonase; Claritin (Gliclazide)



Adverse event in 57 year old female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-04-30

Patient: 57 year old female, weighing 68.0 kg (149.6 pounds)

Adverse reactions / side effects: Fatigue, Dizziness, Ulcer, Gastritis

Suspect drug(s):
Nexium
    Administration route: Oral
    Indication: Ulcer
    Start date: 2000-01-01
    End date: 2004-01-01

Prevacid
    Start date: 2000-01-01
    End date: 2004-01-01

Aciphex
    Start date: 2000-01-01
    End date: 2004-01-01

Other drugs received by patient: Zantac



Adverse event in 57 year old male receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from United States on 2007-04-27

Patient: 57 year old male, weighing 124.7 kg (274.3 pounds)

Adverse reactions / side effects: Neuropathy, Rash Generalised, Skin Exfoliation, Diabetes Mellitus, Condition Aggravated, Fall, Loss of Consciousness, Renal Failure, Skin Laceration, Oedema Peripheral, Dehydration, Dizziness, Tenderness, Influenza Like Illness

Adverse event resulted in: hospitalization

Suspect drug(s):
Prevacid (Lansoprazole)

Other drugs received by patient: Prinivil; Topamax; Aspirin; Lipitor; Byetta; Glucophage; Glucotrol; Actos; Plavix; Pepcid



Adverse event in 12 year old female receiving Prevacid (Lansoprazole)

Reported by a consumer/non-health professional from United States on 2007-02-20

Patient: 12 year old female

Adverse reactions / side effects: Colour Blindness, Dizziness, Blindness, Loss of Consciousness

Suspect drug(s):
Zantac
    Dosage: 150mg per day
    Administration route: Oral
    Indication: Gastrooesophageal Reflux Disease
    Start date: 2006-05-22
    End date: 2006-06-08

Prevacid
    Dosage: 30mg per day
    Start date: 2006-05-22
    End date: 2006-06-08

Other drugs received by patient: NO Concurrent Medication



Adverse event in female receiving Prevacid (Lansoprazole)

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 Prevacid (Lansoprazole)

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



Adverse event in 54 year old female receiving Prevacid (Lansoprazole)

Reported by a individual with unspecified qualification from Canada on 2007-01-29

Patient: 54 year old female

Adverse reactions / side effects: Confusional State, Drug Dose Omission, Dyspnoea, Wrong Drug Administered, Tachycardia, Drug Interaction, Blood Calcium Increased, Drug Withdrawal Syndrome, Headache, Gastric Haemorrhage, Haemoglobin Decreased, Medication Error, Dizziness

Adverse event resulted in: hospitalization

Suspect drug(s):
Effexor XR
    Dosage: 75 mg 1x per 1 day
    Administration route: Oral
    Indication: Anxiety
    Start date: 2002-01-01

Effexor XR
    Dosage: 75 mg 1x per 1 day
    Administration route: Oral
    Indication: Panic Attack
    Start date: 2002-01-01

Effexor XR
    Dosage: 75 mg 1x per 1 day
    Administration route: Oral
    Indication: Post-Traumatic Stress Disorder
    Start date: 2002-01-01

Pantoloc (Pantoprazole, Tablet, Delayed Release, 0)
    Indication: Gastric Haemorrhage

Prevacid
    Dosage: 30 mg qam
    Administration route: Oral
    Indication: Gastric Haemorrhage
    Start date: 2006-11-13
    End date: 2006-12-12

Other drugs received by patient: Ativan; Naproxen

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