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Index of reports
> Cases resulting in a serious event (27)
> Cases with Dizziness (5)
Below is the selection of adverse event reports related to Prevacid (Lansoprazole) that includes cases resulting in a serious event where reactions include dizziness.
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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