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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Allegra (Fexofenadine). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (65)
Cases resulting in a serious event (55)
Cases resulting in life threatening events (4)
Cases resulting in hospitalization (23)
Cases resulting in disability (3)
Cases resulting in other serious reactions (32)
Below is a sample of reports where side effects / adverse reactions may be related to Allegra (Fexofenadine). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 2 year old male receiving Allegra (Fexofenadine)
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: 2 year old male
Adverse reactions / side effects: Anaphylactic Reaction
Suspect drug(s):
Allegra
Indication: Drug USE FOR Unknown Indication
Miralax
Dosage: po
Administration route: Oral
Indication: Constipation
Start date: 2006-06-01
End date: 2007-10-17
Neocate
Indication: Drug USE FOR Unknown Indication
Prevacid
Indication: Drug USE FOR Unknown Indication
Pulmicort
Indication: Drug USE FOR Unknown Indication
Singulair
Indication: Drug USE FOR Unknown Indication
Adverse event in female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-10-24
Patient: female, weighing 50.0 kg (110.0 pounds)
Adverse reactions / side effects: Asthma, Blood Creatine Phosphokinase Increased, Cardiac Failure, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Start date: 2007-05-31
End date: 2007-06-19
Crestor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-05-31
End date: 2007-06-14
Relifen
Administration route: Oral
Start date: 2006-12-01
Spiriva
Indication: Bronchitis Chronic
Start date: 2007-05-31
Other drugs received by patient: Almeta; Aldactone; Famotidine; SM; Elieten; Lasix; Gosha-Jinki-GAN; Acardi; Solon; NU-Lotan; Bezatol SR; Uralyt-U; Restamin; Transamin; Hustagin; Meiact; Mohrus Tape; Urepearl; Nitropen; Buscopan; Epadel S; Frandol S; Antibiotic Preparations Acting Mainly ON Gram Positive BA
Adverse event in female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-10-10
Patient: female, weighing 50.0 kg (110.0 pounds)
Adverse reactions / side effects: Asthma, Blood Creatine Phosphokinase Increased, Chest Discomfort, Cardiac Failure, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Start date: 2007-05-31
End date: 2007-06-19
Crestor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-05-31
End date: 2007-06-14
Relifen
Administration route: Oral
Start date: 2006-12-01
Spiriva
Indication: Bronchitis Chronic
Start date: 2007-05-31
Other drugs received by patient: Almeta; Aldactone; Famotidine; SM; Elieten; Lasix; Gosha-Jinki-GAN; Acardi; Solon; NU-Lotan; Bezatol SR; Uralyt-U; Restamin; Transamin; Hustagin; Meiact; Mohrus Tape; Urepearl; Nitropen; Buscopan; Epadel S; Frandol S; Antibiotic Preparations Acting Mainly ON Gram Positive BA
Adverse event in 67 year old female receiving Allegra (Fexofenadine)
Reported by a pharmacist from Japan on 2007-10-02
Patient: 67 year old female
Adverse reactions / side effects: Malaise, Chest Discomfort, Hepatic Function Abnormal
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Herbal Preparation
Adverse event in 12 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-31
Patient: 12 year old female, weighing 47.0 kg (103.4 pounds)
Adverse reactions / side effects: Drug Eruption, Conjunctivitis, Erythema Multiforme
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Azeptin / 00884001 /; Locoid; Dermovate; Vaseline / 01007601 /
Adverse event in 20 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-31
Patient: 20 year old male
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Celtect
Adverse event in 30 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-26
Patient: 30 year old female
Adverse reactions / side effects: Amnesia, Loss of Consciousness
Suspect drug(s):
Allegra (Fexofenadine)
Adverse event in 35 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-26
Patient: 35 year old female, weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Jaundice, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Meiact; Selbex; Podonin S; Nauzelin
Adverse event in 12 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-25
Patient: 12 year old female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Tonic Convulsion, Disorientation, Altered State of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Depakene / 00228502 /; Phenobal / 00023201 /
Adverse event in male receiving Allegra (Fexofenadine)
Reported by a physician from United States on 2007-07-25
Patient: male, weighing 82.6 kg (181.7 pounds)
Adverse reactions / side effects: Chronic Fatigue Syndrome, Colonic Polyp, Hungry Bone Syndrome, Dyspepsia, Arteriosclerosis, Autonomic Nervous System Imbalance, Hypothermia, Osteopenia, Nasal Congestion, Diverticulum, Sleep Disorder, Left Atrial Dilatation, Nasal Cyst, Thyroid Neoplasm, Sleep Apnoea Syndrome, Atelectasis, Nasal Turbinate Hypertrophy, Vasomotor Rhinitis, Myalgia, Weight Increased, Exostosis, Hypersomnia, Renal Disorder, Bone Lesion, Haemorrhoids, Dental Caries, Rhinorrhoea, Cognitive Disorder, Arrhythmia, Parathyroid Tumour Benign, Spinal Osteoarthritis, Drug Dependence
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Dosage: daily dose:180mg
Astelin
Indication: Rhinitis
Start date: 1994-01-01
End date: 2007-06-28
Dextroamphetamine Sulfate
Lipitor
Indication: Hypercholesterolaemia
Start date: 2006-01-01
Propofol
Xalatan
Indication: Glaucoma
Other drugs received by patient: Synthroid; Vitamin D3; Aspirin; Thyroxin; Hepatitis B Vaccine; Levothyroxine Sodium; Dextroamphetamine Sulfate; Methylphenidate HCL; Ascorbic Acid; Vitamin B; Vitamin CAP; Calcium Chloride; Coffee; Atrovent; Nasalcrom; Montelukast Sodium; Sudafed 12 Hour; Oxymetazoline Hydrochloride; Levopropylhexedrine; Zocor; Zetia; Mevacor; ALL Other Therapeutic Products
Adverse event in receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-23
Patient:
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra
Administration route: Oral
Celtect
Adverse event in 50 year old female receiving Allegra (Fexofenadine)
Reported by a individual with unspecified qualification from United States on 2007-07-19
Patient: 50 year old female, weighing 109.8 kg (241.5 pounds)
Adverse reactions / side effects: Drug Ineffective, Gastrooesophageal Reflux Disease
Suspect drug(s):
Allegra (Fexofenadine)
Adverse event in 17 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-16
Patient: 17 year old female
Adverse reactions / side effects: Hypotension, Shock
Suspect drug(s):
Allegra (Fexofenadine)
Adverse event in receiving Allegra (Fexofenadine)
Reported by a pharmacist from Japan on 2007-07-10
Patient:
Adverse reactions / side effects: Pancytopenia
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Unknown Drug
Adverse event in 51 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-06
Patient: 51 year old female, weighing 46.0 kg (101.2 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal, C-Reactive Protein Increased, Pyrexia, White Blood Cell Count Increased, Hepatocellular Damage
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Rinderon / 00008501 /; Hirudoid / 00723701 /
Adverse event in 12 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-05
Patient: 12 year old female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Tonic Convulsion, Disorientation, Altered State of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Depakene / 00228502 /; Phenobal / 00023201 /
Adverse event in male receiving Allegra (Fexofenadine)
Reported by a consumer/non-health professional from United States on 2007-07-02
Patient: male, weighing 79.4 kg (174.6 pounds)
Adverse reactions / side effects: Palpitations
Suspect drug(s):
Allegra (Fexofenadine)
Adverse event in 17 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-07-02
Patient: 17 year old male
Adverse reactions / side effects: Rhabdomyolysis
Suspect drug(s):
Allegra
Administration route: Oral
Start date: 2007-04-28
End date: 2007-04-29
Gatifloxacin
Start date: 2007-04-28
End date: 2007-04-29
Loxonin / 00890701 /
Start date: 2007-04-28
End date: 2007-04-29
Onon
Start date: 2007-04-28
End date: 2007-04-29
Other drugs received by patient: Tamiflu
Adverse event in 70 year old female receiving Allegra (Fexofenadine)
Reported by a pharmacist from Japan on 2007-06-29
Patient: 70 year old female
Adverse reactions / side effects: Retinal Haemorrhage
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Clarithromycin; Mucodyne; Interferon
Adverse event in 51 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-06-25
Patient: 51 year old female, weighing 46.0 kg (101.2 pounds)
Adverse reactions / side effects: Hepatic Function Abnormal, Pyrexia, Hepatocellular Damage
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Rinderon / 00008501 /; Hirudoid / 00723701 /
Adverse event in 13 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-06-12
Patient: 13 year old female
Adverse reactions / side effects: Conjunctivitis, Erythema Multiforme
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Azeptin / 00884001 /; Azeptin / 00884001 /
Adverse event in 17 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-06-08
Patient: 17 year old male
Adverse reactions / side effects: Rhabdomyolysis
Suspect drug(s):
Allegra
Administration route: Oral
Loxonin / 00890701 /
Onon
Other drugs received by patient: Gatifloxacin; Tamiflu
Adverse event in 51 year old female receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-06-08
Patient: 51 year old female
Adverse reactions / side effects: C-Reactive Protein Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Pyrexia
Adverse event resulted in: hospitalization
Suspect drug(s):
Allegra (Fexofenadine)
Other drugs received by patient: Rinderon / 00008501 /
Adverse event in 50 year old female receiving Allegra (Fexofenadine)
Reported by a individual with unspecified qualification from United States on 2007-06-08
Patient: 50 year old female, weighing 109.8 kg (241.5 pounds)
Adverse reactions / side effects: Therapeutic Response Unexpected With Drug Substitution, Drug Ineffective
Suspect drug(s):
Allegra (Fexofenadine)
Adverse event in 17 year old male receiving Allegra (Fexofenadine)
Reported by a physician from Japan on 2007-05-18
Patient: 17 year old male
Adverse reactions / side effects: Rhabdomyolysis
Suspect drug(s):
Allegra
Administration route: Oral
Loxonin / 00890701 /
Onon
Other drugs received by patient: Gatifloxacin; Tamiflu
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