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Index of reports
> Cases resulting in other serious reactions (41)
Below is the selection of adverse event reports related to Ranitidine that includes cases resulting in other serious reactions.
Reports 1 - 25 of 41 Next >>
Adverse event in female receiving Ranitidine
Reported by a pharmacist from Germany on 2007-10-29
Patient: female
Adverse reactions / side effects: Dysgeusia, Neurotoxicity, Malaise, Nail Disorder, Abdominal Pain Upper
Suspect drug(s):
Gabapentin
Dosage: text:0.5 tablet
Administration route: Oral
Indication: Neurotoxicity
Carboplatin
Dosage: daily dose:500mg
Indication: Chemotherapy
Paclitaxel
Dosage: daily dose:294mg
Indication: Fallopian Tube Cancer
Start date: 2007-06-20
End date: 2007-10-04
Ranitidine
Indication: Prophylactic Chemotherapy
Start date: 2007-06-20
End date: 2007-10-04
Adverse event in female receiving Ranitidine
Reported by a pharmacist from Germany on 2007-10-26
Patient: female
Adverse reactions / side effects: Neurotoxicity, Dysgeusia, Malaise, Nail Disorder, Abdominal Pain Upper
Suspect drug(s):
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-06-20
End date: 2007-06-20
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-07-11
End date: 2007-07-11
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-08-01
End date: 2007-08-01
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-08-22
End date: 2007-08-22
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-09-12
End date: 2007-09-12
Ranitidine
Dosage: see image
Indication: Prophylaxis
Start date: 2007-10-04
End date: 2007-10-04
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-06-20
End date: 2007-06-20
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-07-11
End date: 2007-07-11
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-08-01
End date: 2007-08-01
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-08-22
End date: 2007-08-22
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-09-12
End date: 2007-09-12
Carboplatin
Dosage: see image
Indication: Chemotherapy
Start date: 2007-10-04
End date: 2007-10-04
Gabapentin
Dosage: oral
Administration route: Oral
Indication: Neurotoxicity
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-06-20
End date: 2007-06-20
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-07-11
End date: 2007-07-11
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-08-01
End date: 2007-08-01
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-08-22
End date: 2007-08-22
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-09-12
End date: 2007-09-12
Paclitaxel
Dosage: see image
Indication: Fallopian Tube Cancer
Start date: 2007-10-04
End date: 2007-10-04
Other drugs received by patient: Sodium Chloride (Sodium Chloride) Solution FOR Infusion, 0.9%; Tropisetron (Tropisetron); Metoclopramide (Metoclopramide)
Adverse event in 16 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-05
Patient: 16 year old male
Adverse reactions / side effects: Injection Site Erythema, Medication Error
Suspect drug(s):
Ranitidine
Adverse event in 44 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-12
Patient: 44 year old male
Adverse reactions / side effects: Dermatitis Contact
Suspect drug(s):
Ranitidine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-07-11
Patient:
Adverse reactions / side effects: Sepsis Neonatal
Suspect drug(s):
Ranitidine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-07-11
Patient:
Adverse reactions / side effects: Sepsis Neonatal
Suspect drug(s):
Ranitidine
Adverse event in receiving Ranitidine
Reported by a pharmacist from United States on 2007-06-22
Patient:
Adverse reactions / side effects: Medication Error
Suspect drug(s):
Paroxetine
Ranitidine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-06-21
Patient:
Adverse reactions / side effects: Cholestasis, Mixed Hepatocellular-Cholestatic Injury, Hepatocellular Damage
Suspect drug(s):
Nimesulide
Acetylsalicylic Acid SRT
Dosage: median 500 mg (500 - 2500 mg)
Ranitidine
Hydrochlorothiazide
Tranxene
Paracetamol
Dosage: median 650 mg (min. 500 mg, max. 3250 mg)
Metamizole
Budesonide
Naproxen
Ipratropium Bromide
Other Drugs and Herbs
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-06-19
Patient:
Adverse reactions / side effects: Drug Interaction, Myocarditis
Suspect drug(s):
Ranitidine
Clozapine
Adverse event in receiving Ranitidine
Reported by a individual with unspecified qualification on 2007-06-19
Patient:
Adverse reactions / side effects: Drug Interaction, Myocarditis
Suspect drug(s):
Ranitidine
Paracetamol
Sertraline
Clozapine
Adverse event in 86 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-18
Patient: 86 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Gabapentin
Dosage: see image
Administration route: Oral
Start date: 2006-09-06
End date: 2007-03-13
Gabapentin
Dosage: see image
Administration route: Oral
Start date: 2007-04-05
End date: 2007-04-13
Ranitidine
Dosage: 150 mg, bid, oral
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Other drugs received by patient: Bendroflumethiazide (Bendroflumethiazide); Diclofenac (Diclofenac); Domperidone (Domperidone); Levothyroxine Sodium; Movicol; Oxycontin
Adverse event in 88 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-15
Patient: 88 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Gabapentin
Administration route: Oral
Start date: 2006-09-06
End date: 2007-04-13
Ranitidine
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Other drugs received by patient: Bendroflumethiazide; Diclofenac; Domperidone; Levothyroxine Sodium; Movicol; Oxycontin
Adverse event in 88 year old female receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-06-11
Patient: 88 year old female
Adverse reactions / side effects: Mania, Paranoia, Cerebellar Ataxia
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Ranitidine
Dosage: 150mg twice per day
Administration route: Oral
Start date: 2007-03-27
End date: 2007-04-10
Gabapentin
Administration route: Oral
Start date: 2006-09-06
End date: 2007-04-13
Other drugs received by patient: Bendroflumethiazide; Diclofenac; Domperidone; Levothyroxine Sodium; Movicol; Oxycontin
Adverse event in 52 year old female receiving Ranitidine
Reported by a physician from Argentina on 2007-05-25
Patient: 52 year old female
Adverse reactions / side effects: Renal Failure, Skin Exfoliation, Intentional Self-Injury, Rash Pruritic
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Eskalith
Dosage: 900mg per day
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2007-04-27
End date: 2007-05-10
Lamotrigine
Dosage: 150mg per day
Administration route: Oral
Indication: Bipolar Disorder
Start date: 2006-07-01
End date: 2007-04-27
Ranitidine
Indication: Drug USE FOR Unknown Indication
Levothyroxine Sodium
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: NO Concurrent Medication
Adverse event in female receiving Ranitidine
Reported by a lawyer from United States on 2007-05-18
Patient: female
Adverse reactions / side effects: Intentional Overdose, Drug Ineffective, Suicide Attempt, Self Injurious Behaviour
Suspect drug(s):
Neurontin
Indication: Back Pain
Neurontin
Indication: Arthralgia
Lipitor
Hydrochlorothiazide
Ranitidine
Other drugs received by patient: Carisoprodol; Celebrex; Hydrocodone Bitartrate; Amitriptyline HCL
Adverse event in 43 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-17
Patient: 43 year old male
Adverse reactions / side effects: Suicide Attempt, Multiple Drug Overdose, Lethargy
Suspect drug(s):
Tramadol HCL
Administration route: Oral
Indication: Intentional Drug Misuse
Acetaminophen W / Propoxyphene HCL
Administration route: Oral
Indication: Intentional Drug Misuse
Ssri
Administration route: Oral
Indication: Drug Abuser
Ranitidine
Administration route: Oral
Indication: Drug Abuser
Atypical Antipsychotic
Administration route: Oral
Indication: Drug Abuser
Methacarbanol
Administration route: Oral
Indication: Drug Abuser
Benzodiazepine
Administration route: Oral
Indication: Drug Abuser
Adverse event in 40 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-17
Patient: 40 year old male
Adverse reactions / side effects: Dermatitis Contact
Suspect drug(s):
Ranitidine
Adverse event in 44 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-15
Patient: 44 year old male
Adverse reactions / side effects: Dermatitis Contact
Suspect drug(s):
Ranitidine
Adverse event in 31 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-15
Patient: 31 year old male
Adverse reactions / side effects: Myalgia, Pneumonia, Malaise, Pleurisy, Lower Respiratory Tract Infection
Adverse event resulted in: death
Suspect drug(s):
Ranitidine
Dosage: 150 mg, qd, oral
Administration route: Oral
Indication: Dyspepsia
Clozaril
Dosage: 275 mg, qd, oral
Administration route: Oral
Indication: Schizophrenia
Start date: 2007-03-29
Venlafaxine HCL
Dosage: 225 mg, qd, oral
Administration route: Oral
Indication: Depression
Other drugs received by patient: Beclomethasone Dipropionate; Dihydrocodeine Compound; Salbutamol (Salbutamol)
Adverse event in 31 year old male receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-05-09
Patient: 31 year old male
Adverse reactions / side effects: Neutrophil Count Increased, Pneumonia, Pleurisy, Lower Respiratory Tract Infection, Death, Myalgia, Malaise, White Blood Cell Count Increased
Adverse event resulted in: death
Suspect drug(s):
Ranitidine
Dosage: 150mg per day
Administration route: Oral
Indication: Dyspepsia
Clozaril
Dosage: 275mg per day
Administration route: Oral
Indication: Schizophrenia
Start date: 2006-03-29
Venlafaxine HCL
Dosage: 225mg per day
Administration route: Oral
Indication: Depression
Other drugs received by patient: Beclomethasone Dipropionate; Dihydrocodeine Bitartrate INJ; Salbutamol; Antibiotic
Adverse event in 31 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-09
Patient: 31 year old male
Adverse reactions / side effects: Myalgia, Death, Pneumonia, Malaise, Pleurisy, Lower Respiratory Tract Infection
Adverse event resulted in: death
Suspect drug(s):
Venlafaxiine HCL
Administration route: Oral
Indication: Depression
Clozaril
Administration route: Oral
Indication: Schizophrenia
Start date: 2006-03-29
Ranitidine
Administration route: Oral
Indication: Dyspepsia
Other drugs received by patient: Salbutamol; Beclomethasone Dipropionate; Dihydrocodeine Bitartrate INJ
Adverse event in 32 year old female receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-23
Patient: 32 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Rash Generalised, Drug Exposure During Pregnancy, Urticaria, Throat Tightness
Adverse event resulted in: life threatening event
Suspect drug(s):
Ranitidine
Adverse event in 54 year old male receiving Ranitidine
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-04-19
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Hypotension, Anaesthetic Complication
Suspect drug(s):
Midazolam Hydrochloride
Dosage: 1 mg, once, intravenous
Start date: 2007-02-22
Propofol
Dosage: 1 df, once, intravenous
Start date: 2007-02-22
Dexamethasone TAB
Dosage: 4 mg, once, intravenous
Start date: 2007-02-22
Ketoprofen
Dosage: 100 mg, once, oral
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Oxygen (Oxygen)
Start date: 2007-02-22
Ranitidine
Dosage: 150 mg, oral
Administration route: Oral
Remifentanil (Remifentanil)
Dosage: 1 df, once, intravenous
Start date: 2007-02-22
Tramadol HCL
Dosage: 100 mg, once, intravenous
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Acetaminophen; Hartman's (Ringer-Lactate Solution (Fresenius); Chlorhexidine (Chlorhexidine); Marcaine
Adverse event in 54 year old male receiving Ranitidine
Reported by a consumer/non-health professional from United Kingdom on 2007-04-18
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Restlessness, Hypotension
Suspect drug(s):
Ranitidine
Administration route: Oral
Indication: Premedication
Remifentanil
Start date: 2007-02-22
Dexamethasone 0.5mg TAB
Dosage: 4mg per day
Start date: 2007-02-22
Ketoprofen
Dosage: 100mg per day
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Midazolam HCL
Dosage: 1mg per day
Start date: 2007-02-22
Oxygen
Start date: 2007-02-22
Propofol
Start date: 2007-02-22
Tramadol HCL
Dosage: 100mg per day
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Paracetamol
Adverse event in 54 year old male receiving Ranitidine
Reported by a individual with unspecified qualification from United Kingdom on 2007-04-18
Patient: 54 year old male, weighing 113.0 kg (248.6 pounds)
Adverse reactions / side effects: PO2 Decreased, Vomiting, Diarrhoea, Hypotension
Suspect drug(s):
Dexamethasone
Dosage: 4 milligrams; daily; intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Ketoprofen
Dosage: 100 milligrams; daily, oral
Administration route: Oral
Indication: Premedication
Start date: 2007-02-22
End date: 2007-02-22
Midazolam HCL
Dosage: 1 milligrams; daily, intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Oxygen (Oxygen)
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Propofol
Dosage: 1 dose form; daily; intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Ranitidine
Dosage: 150 milligrams; unknown; oral
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Remifentanil (Remifentanil)
Dosage: 1 dose form; daily; intravenous
Indication: Drug USE FOR Unknown Indication
Start date: 2007-02-22
Tramadol HCL
Dosage: 100 milligrams; daily; intravenous
Indication: Perioperative Analgesia
Start date: 2007-02-22
End date: 2007-02-22
Other drugs received by patient: Chlorpheniramine Maleate; Felodipine; Ibuprofen; Paracetamol
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