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This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Claritin (Loratadine). 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 (99)
Cases resulting in a serious event (97)
Cases resulting in death (1)
Cases resulting in life threatening events (1)
Cases resulting in hospitalization (19)
Cases resulting in other serious reactions (83)
Below is a sample of reports where side effects / adverse reactions may be related to Claritin (Loratadine). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 50 year old male receiving Claritin (Loratadine)
Reported by a physician from Japan on 2007-10-29
Patient: 50 year old male
Adverse reactions / side effects: Malaise, Nausea, Hypotension, Dizziness, Cold Sweat, Asthenia
Suspect drug(s):
Claritin (Loratadine)
Adverse event in 4 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from Brazil on 2007-10-29
Patient: 4 year old female, weighing 18.0 kg (39.6 pounds)
Adverse reactions / side effects: Acute Sinusitis, Hypothermia
Adverse event resulted in: hospitalization
Suspect drug(s):
Claritin
Dosage: 2.5 ml; qd; po
Administration route: Oral
Indication: Hypersensitivity
Start date: 2007-10-07
End date: 2007-10-14
Novalgina (Metamizole Sodium)
Dosage: ; qid; po
Administration route: Oral
Indication: Sinusitis
Adverse event in 48 year old male receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-10-18
Patient: 48 year old male, weighing 122.5 kg (269.4 pounds)
Adverse reactions / side effects: Hypertension
Suspect drug(s):
Claritin
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-10-01
Claritin-D 24 Hour
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Nasopharyngitis
Start date: 2007-09-01
End date: 2007-10-02
Other drugs received by patient: Advair (Con.); Flonase (Con.)
Adverse event in 97 year old male receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-10-11
Patient: 97 year old male, weighing 64.9 kg (142.7 pounds)
Adverse reactions / side effects: Malaise, Chest Discomfort, Angina Pectoris
Suspect drug(s):
Claritin (Loratadine)
Other drugs received by patient: Plavix; Lipitor; Toprol-XL
Adverse event in receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-10-11
Patient:
Adverse reactions / side effects: Pharyngeal Oedema
Suspect drug(s):
Claritin
Dosage: po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Singulair
Indication: Drug USE FOR Unknown Indication
Adverse event in receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-10-10
Patient:
Adverse reactions / side effects: Pharyngeal Oedema
Suspect drug(s):
Claritin
Administration route: Oral
Singulair
Administration route: Oral
Adverse event in 28 year old male receiving Claritin (Loratadine)
Reported by a physician from Japan on 2007-10-10
Patient: 28 year old male, weighing 58.0 kg (127.6 pounds)
Adverse reactions / side effects: Dermatitis Atopic, Generalised Erythema, Joint Swelling, Ocular Hyperaemia, Condition Aggravated, Upper Respiratory Tract Inflammation, Erythema Multiforme
Adverse event resulted in: hospitalization
Suspect drug(s):
Bufferin A (Bufferin A)
Dosage: 1 df; ; po
Administration route: Oral
Indication: Headache
End date: 2007-07-28
Claritin
Dosage: 10 mg; ; po
Administration route: Oral
Indication: Pruritus
End date: 2007-07-29
EVE Quick (NO Pref. Name)
Dosage: 1 df; ; po
Administration route: Oral
Indication: Headache
Tavegyl (NO Pref. Name)
Dosage: 1 df; ; po
Indication: Pruritus
Adverse event in receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-10-01
Patient:
Adverse reactions / side effects: Pharyngeal Oedema
Suspect drug(s):
Claritin (Loratadine)
Adverse event in female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-23
Patient: female
Adverse reactions / side effects: Pharyngeal Oedema, Face Oedema, Eye Oedema, Headache
Suspect drug(s):
Claritin (Loratadine)
Adverse event in 65 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-23
Patient: 65 year old female, weighing 64.0 kg (140.7 pounds)
Adverse reactions / side effects: Confusional State, Hypersensitivity, Pruritus, Urticaria, Loss of Consciousness, Burning Sensation, Road Traffic Accident, Fatigue, Rash Erythematous, Pharmaceutical Product Complaint, Blister
Suspect drug(s):
Ambien CR
Indication: Insomnia
Start date: 2001-01-01
Claritin
Dosage: 1 df;qd;po
Administration route: Oral
Indication: Lacrimation Increased
Start date: 2007-05-14
End date: 2007-05-17
Claritin
Dosage: 1 df;qd;po
Administration route: Oral
Indication: Rhinorrhoea
Start date: 2007-05-14
End date: 2007-05-17
Detrol LA
Indication: Hypertonic Bladder
Start date: 2002-01-01
Lipitor
Dosage: 10 mg;
Indication: Blood Cholesterol Increased
Start date: 2004-01-01
Wellbutrin
Indication: Depression
Start date: 2001-01-01
Other drugs received by patient: Estrogen NOS
Adverse event in receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-20
Patient:
Adverse reactions / side effects: Pharyngeal Oedema
Suspect drug(s):
Claritin (Loratadine)
Adverse event in 61 year old male receiving Claritin (Loratadine)
Reported by a physician from Japan on 2007-07-20
Patient: 61 year old male
Adverse reactions / side effects: Impaired Driving Ability, Drug Effect Decreased, Road Traffic Accident, Somnolence
Suspect drug(s):
Claritin
Dosage: see image
Administration route: Oral
Indication: Urticaria
Start date: 2007-03-10
End date: 2007-06-25
Claritin
Dosage: see image
Administration route: Oral
Indication: Urticaria
Start date: 2007-06-26
End date: 2007-07-04
Other drugs received by patient: Zantac 150; Atarax
Adverse event in 69 year old male receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-18
Patient: 69 year old male
Adverse reactions / side effects: Blood Glucose Decreased
Suspect drug(s):
Avandryl
Dosage: ;po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Claritin
Dosage: ;po
Administration route: Oral
Indication: Lacrimation Increased
Start date: 2007-06-30
End date: 2007-07-01
Claritin
Dosage: ;po
Administration route: Oral
Indication: Sneezing
Start date: 2007-06-30
End date: 2007-07-01
Claritin
Dosage: ;po
Administration route: Oral
Indication: Throat Irritation
Start date: 2007-06-30
End date: 2007-07-01
Insulin
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Tarka; Hydrochlorothiazide; Lipitor; Indomethacin; Metoprolol Succinate
Adverse event in 6 year old male receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-18
Patient: 6 year old male, weighing 20.4 kg (44.9 pounds)
Adverse reactions / side effects: Abnormal Behaviour, Aggression
Suspect drug(s):
Claritin (Loratadine)
Adverse event in 91 year old female receiving Claritin (Loratadine)
Reported by a physician from Japan on 2007-07-18
Patient: 91 year old female, weighing 44.1 kg (97.0 pounds)
Adverse reactions / side effects: Ventricular Tachycardia, Anorexia, Dementia, Cardiac Failure Congestive
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Claritin
Dosage: 10 mg; ; po
Administration route: Oral
Indication: Impetigo
Start date: 2007-04-30
End date: 2007-05-18
Claritin
Dosage: 10 mg; ; po
Administration route: Oral
Indication: Pruritus
Start date: 2007-04-30
End date: 2007-05-18
Minocycline HCL
Dosage: 100 mg;qd;po
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2007-05-02
End date: 2007-05-16
Other drugs received by patient: Gentacin; Rinderon
Adverse event in 62 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from Canada on 2007-07-16
Patient: 62 year old female
Adverse reactions / side effects: Myalgia, Chest Pain, Throat Tightness
Suspect drug(s):
Claritin (Loratadine)
Adverse event in 63 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: 63 year old female, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Glaucoma, Mydriasis, Conjunctivitis, Retinal Disorder
Suspect drug(s):
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Hypersensitivity
Start date: 2005-01-01
End date: 2007-06-17
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Lacrimation Increased
Start date: 2005-01-01
End date: 2007-06-17
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Sneezing
Start date: 2005-01-01
End date: 2007-06-17
Claritin
Dosage: po
Administration route: Oral
Indication: Lacrimation Increased
End date: 2007-06-15
Claritin
Dosage: po
Administration route: Oral
Indication: Sneezing
End date: 2007-06-15
Sudafed 12 Hour
Dosage: po
Administration route: Oral
Indication: Lacrimation Increased
Sudafed 12 Hour
Dosage: po
Administration route: Oral
Indication: Sneezing
Other drugs received by patient: Glaucoma Medication
Adverse event in 90 year old receiving Claritin (Loratadine)
Reported by a physician from Japan on 2007-07-11
Patient: 90 year old
Adverse reactions / side effects: Ventricular Arrhythmia
Adverse event resulted in: hospitalization
Suspect drug(s):
Claritin (Loratadine)
Other drugs received by patient: Minomycin (Con.)
Adverse event in male receiving Claritin (Loratadine)
Reported by a health professional (non-physician/pharmacist) from Poland on 2007-07-11
Patient: male
Adverse reactions / side effects: Dyspnoea
Suspect drug(s):
Claritin (Loratadine)
Other drugs received by patient: Diphergan / 00033002 / (Con.)
Adverse event in 53 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-11
Patient: 53 year old female, weighing 63.5 kg (139.7 pounds)
Adverse reactions / side effects: Dyspnoea, Malaise, NO Therapeutic Response, Condition Aggravated, Multiple Allergies, Throat Tightness
Suspect drug(s):
Claritin
Dosage: 1 df; po
Administration route: Oral
Indication: Multiple Allergies
Start date: 2007-05-01
End date: 2007-05-01
Claritin
Dosage: 1 df; po
Administration route: Oral
Indication: Rhinorrhoea
Start date: 2007-05-01
End date: 2007-05-01
Claritin
Dosage: 1 df; po
Administration route: Oral
Indication: Sneezing
Start date: 2007-05-01
End date: 2007-05-01
Adverse event in 63 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-05
Patient: 63 year old female
Adverse reactions / side effects: Mydriasis, Glaucoma, Conjunctivitis
Suspect drug(s):
Claritin
Dosage: po
Administration route: Oral
Indication: Lacrimation Increased
End date: 2007-06-15
Claritin
Dosage: po
Administration route: Oral
Indication: Sneezing
End date: 2007-06-15
Claritin
Dosage: po
Administration route: Oral
Indication: Lacrimation Increased
End date: 2007-06-15
Claritin
Dosage: po
Administration route: Oral
Indication: Sneezing
End date: 2007-06-15
Sudafed 12 Hour
Dosage: po
Administration route: Oral
Indication: Lacrimation Increased
Adverse event in 63 year old male receiving Claritin (Loratadine)
Reported by a physician from Japan on 2007-07-05
Patient: 63 year old male
Adverse reactions / side effects: Fistula, Haemorrhoidal Haemorrhage
Suspect drug(s):
Claritin
Dosage: see image
Administration route: Oral
Indication: Eczema
Start date: 2007-05-09
End date: 2007-05-11
Claritin
Dosage: see image
Administration route: Oral
Indication: Eczema
Start date: 2007-05-13
End date: 2007-05-16
Adverse event in 41 year old female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-07-02
Patient: 41 year old female, weighing 45.4 kg (99.8 pounds)
Adverse reactions / side effects: Confusional State, Hypersensitivity, Arthralgia, Dizziness, Metrorrhagia
Suspect drug(s):
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Cough
Start date: 2007-06-07
End date: 2007-06-08
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Hypersensitivity
Start date: 2007-06-07
End date: 2007-06-08
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Nasal Congestion
Start date: 2007-06-07
End date: 2007-06-08
Adverse event in female receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-06-29
Patient: female
Adverse reactions / side effects: Swelling Face, Pharyngeal Oedema, Eye Swelling, Headache
Suspect drug(s):
Claritin (Loratadine)
Adverse event in 3 year old male receiving Claritin (Loratadine)
Reported by a consumer/non-health professional from United States on 2007-06-29
Patient: 3 year old male, weighing 15.4 kg (33.9 pounds)
Adverse reactions / side effects: Irritability, Aggression
Suspect drug(s):
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Hypersensitivity
Start date: 2007-05-04
Claritin
Dosage: 1 df; qd; po
Administration route: Oral
Indication: Rhinorrhoea
Start date: 2007-05-04
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