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Index of reports
> Cases resulting in hospitalization (23)
Below is the selection of adverse event reports related to Zyrtec (Cetirizine) that includes cases resulting in hospitalization.
Adverse event in 15 year old male receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-10-08
Patient: 15 year old male
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Montelukast Sodium
Administration route: Oral
Indication: Asthma
Start date: 2004-03-17
End date: 2007-08-21
Zyrtec
Administration route: Oral
Indication: Dermatitis Atopic
End date: 2007-08-21
Adverse event in male receiving Zyrtec (Cetirizine)
Reported by a physician from United States on 2007-07-24
Patient: male, weighing 6.9 kg (15.2 pounds)
Adverse reactions / side effects: Adrenal Insufficiency Neonatal, Drug Exposure During Pregnancy, Premature Baby, Speech Disorder Developmental, Arnold-Chiari Malformation, Adrenogenital Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Keppra
Dosage: 2000 mg trp
Start date: 2004-09-01
End date: 2005-05-16
Zyrtec
Dosage: 10 mg/d trp
Indication: Hypersensitivity
Dilantin
Dosage: 400 mg/d trp
Dilantin
Dosage: 10 mg 2/d trp
Paxil
Dosage: 37.5 mg/d trp
Indication: Depression
Seroquel
Dosage: 50 mg prn trp
Citrucel
Dosage: ni trp
Folic Acid
Dosage: 4 mg/d trp
Indication: Anaemia
Adverse event in 33 year old female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-07-18
Patient: 33 year old female
Adverse reactions / side effects: Overdose, Suicide Attempt, Coma, Pleural Disorder, Oxygen Saturation Decreased, Loss of Consciousness
Adverse event resulted in: hospitalization
Suspect drug(s):
Citalopram Hydrobromide
Start date: 2006-11-17
End date: 2006-11-17
Acetaminophen
Start date: 2006-11-17
End date: 2006-11-17
Zyrtec
Start date: 2006-11-17
End date: 2006-11-17
Neurontin
Start date: 2006-11-17
End date: 2006-11-17
Prednisone
Start date: 2006-11-17
End date: 2006-11-17
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-07-17
Patient: female
Adverse reactions / side effects: Respiratory Failure, Coma, Suicide Attempt
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zyrtec
Acetaminophen
Acetylcarnitine
Seropram
Prednison
Ecofenac
Adverse event in 33 year old female receiving Zyrtec (Cetirizine)
Reported by a individual with unspecified qualification from Switzerland on 2007-07-16
Patient: 33 year old female
Adverse reactions / side effects: Intentional Overdose, Intubation, Coma, Hypoxia, Suicide Attempt
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Ecofenac (Ngx)(diclofenac) Unknown
Dosage: once/single,
Indication: Suicide Attempt
Start date: 2006-11-17
End date: 2006-11-17
Zyrtec
Dosage: once/single,
Indication: Suicide Attempt
Start date: 2006-11-17
End date: 2006-11-17
Acetaminophen
Dosage: once/single,
Indication: Suicide Attempt
Start date: 2006-11-17
End date: 2006-11-17
Prednisone TAB
Dosage: once/single,
Indication: Suicide Attempt
Start date: 2006-11-17
End date: 2006-11-17
Neurontin
Dosage: once/single,
Indication: Suicide Attempt
Start date: 2006-11-17
End date: 2006-11-17
Citalopram Hydrobromide
Dosage: once/single, urethral
Indication: Suicide Attempt
Start date: 2006-11-17
End date: 2006-11-17
Adverse event in 75 year old female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-04
Patient: 75 year old female
Adverse reactions / side effects: Dermatitis Bullous, Eosinophilia
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Administration route: Oral
Start date: 2006-11-27
End date: 2006-11-28
Dalacine IV
Start date: 2006-11-26
End date: 2006-12-03
Atarax
Administration route: Oral
Start date: 2006-11-29
End date: 2006-12-03
Other drugs received by patient: Oxacillin; Augmentin '125'
Adverse event in 72 year old female receiving Zyrtec (Cetirizine)
Reported by a individual with unspecified qualification from France on 2007-05-02
Patient: 72 year old female
Adverse reactions / side effects: Pruritus, Neutropenia, Hyperthyroidism
Adverse event resulted in: hospitalization
Suspect drug(s):
Keppra
Dosage: 2 g 1/d po
Administration route: Oral
Indication: Convulsion
Start date: 2006-10-26
End date: 2007-02-02
Zyrtec
Dosage: 1 df 1/d po
Administration route: Oral
Indication: Pruritus
Start date: 2006-11-22
End date: 2007-01-23
Depakene
Dosage: 500 mg 1/d
Other drugs received by patient: Rivotril
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from United States on 2007-04-28
Patient: female, weighing 99.8 kg (219.6 pounds)
Adverse reactions / side effects: Marfan's Syndrome, Tinnitus, Contusion, Arterial Disorder, Drug Ineffective, Trigeminal Neuralgia, Pain, Drug Interaction, High Risk Pregnancy, Incontinence, Coronary Artery Occlusion, Blood Cholesterol Increased, Depression, Myocardial Infarction, Fluid Retention, Malaria, Angina Pectoris, Ear Disorder, Ear Infection, Coronary Artery Disease, Uterine Enlargement, Migraine With Aura, Sick Sinus Syndrome, Impaired Healing, Dehydration, Dressler's Syndrome, Multiple Allergies, Hypertension, Neuralgia
Adverse event resulted in: hospitalization
Suspect drug(s):
Celebrex
Indication: Pain
Zyrtec
Relpax
Xalatan
Azithromycin
Other drugs received by patient possibly interacting with the suspect drug:
Lyrica
Indication: Neuralgia
Lasix
Nexium
Other drugs received by patient: Tikosyn; Tikosyn; Atenolol; Plendil; Nitroglycerin; Plavix; Acetylsalicylic Acid SRT; Zetia; Tylenol W / Codeine NO. 3; Zantac; Tetracycline; E-Mycin; Statins; Antidepressants; Antiepileptics; Analgesics; Nitrotab; Penicillin; Clinoril; Demerol; Oxycodone HCL; Darvon; Caffeine; Percocet; Menthol; ALL Other Therapeutic Products; ALL Other Therapeutic Products; Iodine; Sulfonamides; Niacin
Adverse event in 72 year old female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-25
Patient: 72 year old female
Adverse reactions / side effects: Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Dosage: text:1 df
Administration route: Oral
Indication: Pruritus
Start date: 2006-11-22
End date: 2007-01-23
Levetiracetam
Dosage: text:2 g
Administration route: Oral
Indication: Convulsion
Start date: 2006-10-26
End date: 2007-02-02
Valproic Acid
Dosage: daily dose:500mg
Other drugs received by patient: Clonazepam
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-03-23
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Hepatic Cyst, Coma Hepatic, Hepatic Failure, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in 66 year old female receiving Zyrtec (Cetirizine)
Reported by a physician from France on 2007-03-15
Patient: 66 year old female
Adverse reactions / side effects: Drug Ineffective, Prothrombin Time Abnormal, International Normalised Ratio Decreased, Pulmonary Embolism
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Dosage: daily dose:10mg
Administration route: Oral
Indication: Ill-Defined Disorder
Start date: 2004-04-30
End date: 2004-05-07
Quinapril Hydrochloride and Hydrochlorothiazde
Dosage: text:0.5 dose
Administration route: Oral
Indication: Essential Hypertension
Fluindione
Dosage: daily dose:20mg
Administration route: Oral
Indication: Pulmonary Embolism
Start date: 2004-04-28
End date: 2004-05-01
Clonazepam
Dosage: text:0.5 dose
Administration route: Oral
Indication: Ill-Defined Disorder
Soprol
Administration route: Oral
Indication: Essential Hypertension
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-03-15
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Coma Hepatic, Hepatic Failure, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in 38 year old female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Switzerland on 2007-03-14
Patient: 38 year old female
Adverse reactions / side effects: Oligohydramnios, Drug Exposure During Pregnancy, Abortion Induced
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Administration route: Oral
Indication: Urticaria
Lorazepam
Indication: Depression
Fluctine
Administration route: Oral
Indication: Depression
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Italy on 2007-03-13
Patient: female
Adverse reactions / side effects: Electrocardiogram QT Prolonged, Ventricular Tachycardia
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Dosage: daily dose:10mg
Administration route: Oral
Indication: Allergy Prophylaxis
Start date: 2007-02-24
End date: 2007-02-24
Clarithromycin
Dosage: daily dose:1000mg
Administration route: Oral
Indication: Salpingitis
Start date: 2007-02-24
End date: 2007-02-25
Other drugs received by patient: Bromelains
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a consumer/non-health professional from United States on 2007-03-09
Patient: female, weighing 50.8 kg (111.8 pounds)
Adverse reactions / side effects: Hypersensitivity, Nausea, Drug Ineffective, Headache, Convulsion, Liver Disorder, Suicidal Ideation, Weight Increased, Dysstasia, Malaise, Pharyngeal Oedema, Hepatic Cyst, Insomnia, Abdominal Distension, Dizziness, Depression, Oedema Mouth, Feeling Abnormal, Drug Interaction Inhibition
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor
Indication: Blood Cholesterol Increased
Zyrtec
Indication: Multiple Allergies
Xanax
Indication: Depression
Benadryl
Other drugs received by patient possibly interacting with the suspect drug:
Chantix
Indication: Smoking Cessation Therapy
Start date: 2007-02-01
End date: 2007-02-01
Contrast Media
Indication: Computerised Tomogram
Start date: 2007-02-01
End date: 2007-02-01
Other drugs received by patient: Crestor; Zocor; ALL Other Therapeutic Products; Dyazide; Oxygen; Zelnorm; Prevacid
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-03-02
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Coma Hepatic, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-02-26
Patient: female, weighing 40.0 kg (88.0 pounds)
Adverse reactions / side effects: Coma Hepatic, Hepatitis Fulminant
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Dosage: daily dose:5mg
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-09-22
End date: 2007-01-15
Selbex
Dosage: daily dose:150mg
Administration route: Oral
Indication: Gastritis
Start date: 2007-01-07
End date: 2007-01-15
Timepidium Bromide
Dosage: daily dose:90mg
Administration route: Oral
Indication: Gastric Disorder
Start date: 2004-03-24
End date: 2007-01-15
Timepidium Bromide
Indication: Gastritis
Mequitazine
Dosage: daily dose:6mg
Administration route: Oral
Indication: Pruritus
Mequitazine
Loxoprofen Sodium
Dosage: daily dose:180mg
Administration route: Oral
Indication: Back Pain
Start date: 2002-06-21
End date: 2007-01-15
Zyrtec
Dosage: daily dose:5mg
Administration route: Oral
Indication: Pruritus
Start date: 1999-11-12
End date: 2007-01-15
Other drugs received by patient: Magnesium Oxide; Sennosides; Chondnal; Neurotropin
Adverse event in 35 year old female receiving Zyrtec (Cetirizine)
Reported by a physician from United States on 2007-02-16
Patient: 35 year old female
Adverse reactions / side effects: Glaucoma, Abdominal Pain Upper, Tarsal Tunnel Syndrome, Neuropathy Peripheral, Malaise, Thrombophlebitis Superficial, Dizziness, Bronchospasm, Resorption Bone Increased, Blood Creatinine Increased, Cough, Pain in Extremity, Cholelithiasis, Osteoarthritis, Renal Failure, Vestibular Disorder, Vasculitis, Purpura Senile, Bronchitis, Arthritis, Deep Vein Thrombosis, Arthropod Bite, Vertigo Positional
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Advair Diskus 100 / 50
Indication: Drug USE FOR Unknown Indication
Augmentin '125'
Dosage: 1750mg per day
Indication: Drug USE FOR Unknown Indication
Fluticason
Indication: Drug USE FOR Unknown Indication
Bupropion Hydrochloride
Dosage: 300mg unknown
Xanax
Dosage: 1mg three times per day
Indication: Stress
Start date: 1985-01-01
Zyrtec
Indication: Multiple Allergies
Latanoprost
Indication: Drug USE FOR Unknown Indication
Dexamethasone
Indication: Drug USE FOR Unknown Indication
Carisoprodol
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Clotrimazole
Indication: Drug USE FOR Unknown Indication
Clonazepam
Trazodone Hydrochloride
Indication: Drug USE FOR Unknown Indication
Gabapentin
Fluoxetine Hydrochloride
Indication: Drug USE FOR Unknown Indication
Atenolol
Dosage: 50mg per day
Meloxicam
Indication: Drug USE FOR Unknown Indication
Zydone
Indication: Drug USE FOR Unknown Indication
Olmesartan Medoxomil
Dosage: 40mg per day
Allegra D 24 Hour
Indication: Drug USE FOR Unknown Indication
Mometasone Furoate
Indication: Drug USE FOR Unknown Indication
Candesartan Cilexetil
Indication: Drug USE FOR Unknown Indication
Lansoprazole
Indication: Drug USE FOR Unknown Indication
Fluconazole
Indication: Drug USE FOR Unknown Indication
Esomeprazole Magnesium
Indication: Drug USE FOR Unknown Indication
Lotrisone
Indication: Drug USE FOR Unknown Indication
Rizatriptan Benzoate
Indication: Drug USE FOR Unknown Indication
Lomotil
Indication: Drug USE FOR Unknown Indication
Ketoconazole
Dosage: 200mg per day
Indication: Drug USE FOR Unknown Indication
Sinemet
Indication: Drug USE FOR Unknown Indication
Tramadol HCL
Indication: Drug USE FOR Unknown Indication
Metaxalone
Bactrim DS
Dosage: 2u unknown
Indication: Drug USE FOR Unknown Indication
Pethidine Hydrochloride
Indication: Drug USE FOR Unknown Indication
Percocet
Indication: Drug USE FOR Unknown Indication
Codiclear
Indication: Drug USE FOR Unknown Indication
Quinine
Indication: Drug USE FOR Unknown Indication
Moxifloxacin Hydrochloride
Indication: Drug USE FOR Unknown Indication
Rofecoxib
Indication: Drug USE FOR Unknown Indication
Cefazolin
Dosage: 500mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Duratuss
Indication: Drug USE FOR Unknown Indication
Lortab
Indication: Drug USE FOR Unknown Indication
Erythromycin
Dosage: 500mg per day
Indication: Drug USE FOR Unknown Indication
Cephalexin Monohydrate
Dosage: 1500mg per day
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Mupirocin
Administration route: Topical
Indication: Drug USE FOR Unknown Indication
Oseltamivir
Dosage: 150mg per day
Indication: Drug USE FOR Unknown Indication
Endal-HD
Indication: Drug USE FOR Unknown Indication
Triamcinolone Acetonide
Indication: Drug USE FOR Unknown Indication
Omeprazole
Indication: Drug USE FOR Unknown Indication
Exgest LA
Dosage: 2u unknown
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Mescolor
Dosage: 2u unknown
Indication: Drug USE FOR Unknown Indication
Triazolam
Dosage: .25mg per day
Indication: Drug USE FOR Unknown Indication
Lorcet-HD
Dosage: 2u unknown
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Econazole Nitrate
Indication: Drug USE FOR Unknown Indication
Arthrotec
Dosage: 150mg per day
Indication: Drug USE FOR Unknown Indication
Diazepam
Indication: Drug USE FOR Unknown Indication
Celecoxib
Dosage: 200mg per day
Indication: Pain
Sucralfate
Indication: Drug USE FOR Unknown Indication
Lasix
Dosage: 40mg per day
Verapamil
Dosage: 120mg per day
Metoprolol Succinate
Lisinopril
Bisoprolol Fumarate
Amlodipine
Dosage: 5mg per day
Losartan Potassium
Covera-HS
Start date: 2002-01-01
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-02-13
Patient: female
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Dosage: daily dose:10mg
Administration route: Oral
Indication: Dermatitis
Montelukast Sodium
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Difluprednate
Administration route: Topical
Other drugs received by patient: Budesonide
Adverse event in male receiving Zyrtec (Cetirizine)
Reported by a physician from United States on 2007-01-29
Patient: male, weighing 18.1 kg (39.8 pounds)
Adverse reactions / side effects: Obsessive-Compulsive Disorder, Anorexia, Growth Retardation, Tourette's Disorder, Attention Deficit / Hyperactivity Disorder, Sinusitis, Strabismus
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Administration route: Oral
Indication: Hypersensitivity
Zyrtec
Indication: Rhinitis Allergic
Other drugs received by patient: Multi-Vitamins; Focalin
Adverse event in 69 year old female receiving Zyrtec (Cetirizine)
Reported by a physician from Japan on 2007-01-26
Patient: 69 year old female
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Singulair
Administration route: Oral
Indication: Asthma
Start date: 2006-04-17
End date: 2006-05-13
Zyrtec
Administration route: Oral
Indication: Hypersensitivity
Start date: 2006-05-08
End date: 2006-05-13
Other drugs received by patient: Pulmicort; Predonine; Gaslon; Novamin (Prochlorperazine Mesylate); Codeine Phosphate; Magnesium Oxide; Difluprednate
Adverse event in female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from Japan on 2007-01-23
Patient: female
Adverse reactions / side effects: Stevens-Johnson Syndrome
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Dosage: daily dose:10mg-freq:unknown
Administration route: Oral
Indication: Dermatitis
Budesonide
Dosage: text:unknown-freq:unknown
Indication: Drug USE FOR Unknown Indication
Montelukast Sodium
Dosage: text:unknown-freq:unkn0wn
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Difluprednate
Adverse event in 75 year old female receiving Zyrtec (Cetirizine)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-19
Patient: 75 year old female
Adverse reactions / side effects: Dermatitis Bullous, Eosinophilia
Adverse event resulted in: hospitalization
Suspect drug(s):
Zyrtec
Administration route: Oral
Start date: 2006-11-27
End date: 2006-11-28
Dalacine
Administration route: Oral
Start date: 2006-11-26
End date: 2006-12-03
Atarax
Administration route: Oral
Start date: 2006-11-29
End date: 2006-12-03
Other drugs received by patient: Oxacillin
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