|
This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Prednisone. 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 (523)
Cases resulting in a serious event (499)
Cases resulting in death (93)
Cases resulting in life threatening events (26)
Cases resulting in hospitalization (278)
Cases resulting in disability (21)
Cases resulting in other serious reactions (204)
Below is a sample of reports where side effects / adverse reactions may be related to Prednisone. For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in female receiving Prednisone
Reported by a consumer/non-health professional from United States on 2007-10-31
Patient: female
Adverse reactions / side effects: Asthma, Weight Decreased, Pneumonia, Increased Appetite, Nausea, Early Satiety, Abdominal Pain Upper, Tremor, Injection Site Erythema, Diarrhoea, Abdominal Distension, Violence-Related Symptom, Depressed Mood, Blood Glucose Increased, Decreased Appetite
Suspect drug(s):
Nexium
Prednisone
Ranitidine HCL
Symlin
Dosage: 120 mcg;tid;sc
Indication: Diabetes Mellitus
Start date: 2007-01-01
Other drugs received by patient: Prednisone; Nebulizer Treatment, NOT Specified; Antibiotics; Lantus; Glucovance; Avandia; Maalox
Adverse event in male receiving Prednisone
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-10-31
Patient: male
Adverse reactions / side effects: Cataract
Adverse event resulted in: disablity
Suspect drug(s):
Daclizumab(daclizumab)
Dosage: 65 mg, iv nos
Indication: Renal Transplant
Start date: 2004-05-05
End date: 2004-07-01
Mycophenolate Mofetil
Dosage: 1 g, bid, oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2004-05-05
Prednisone
Dosage: 20 mg, oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2004-05-05
Tacrolimus
Dosage: 2.5 mg, oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2004-05-05
Other drugs received by patient: Amlodipine; Sulfamethoxazole; Valganciclovir HCL; Levothyroxine Sodium; Omeprazole; Lorazepam; Glyburide; Losartan Potassium; Rifampicin
Adverse event in male receiving Prednisone
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31
Patient: male
Adverse reactions / side effects: Squamous Cell Carcinoma
Suspect drug(s):
Cortef
Prednisone
Dosage: daily dose:5mg
Saizen
Dosage: daily dose:1.2mg
Indication: Growth Hormone Deficiency
Adverse event in 60 year old male receiving Prednisone
Reported by a individual with unspecified qualification from United States on 2007-10-31
Patient: 60 year old male
Adverse reactions / side effects: Osteonecrosis, Atrial Fibrillation, Osteomyelitis, Cardiac Arrest, Electromechanical Dissociation
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Mycophenolate Mofetil (Mycophenolate Mofetil) Tablet
Dosage: 1000 mg, bid; oral, 2500 mg, uid/qd oral, 1000 mg, uid/qd oral, 500 mg, bid, oral
Administration route: Oral
Indication: Renal Transplant
End date: 2006-04-16
Mycophenolate Mofetil (Mycophenolate Mofetil) Tablet
Dosage: 1000 mg, bid; oral, 2500 mg, uid/qd oral, 1000 mg, uid/qd oral, 500 mg, bid, oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2005-04-05
End date: 2006-12-29
Mycophenolate Mofetil (Mycophenolate Mofetil) Tablet
Dosage: 1000 mg, bid; oral, 2500 mg, uid/qd oral, 1000 mg, uid/qd oral, 500 mg, bid, oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2006-04-20
Prednisone
Dosage: 5 mg, uid/qd; oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2005-04-05
End date: 2007-01-01
Prograf
Dosage: 1 mg, tid; oral, 1.5 mg, uid/qd; oral, 1 mg, bid, oral; 3 mg,uid/qd; oral
Administration route: Oral
Indication: Renal Transplant
End date: 2006-04-17
Prograf
Dosage: 1 mg, tid; oral, 1.5 mg, uid/qd; oral, 1 mg, bid, oral; 3 mg,uid/qd; oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2005-04-05
Prograf
Dosage: 1 mg, tid; oral, 1.5 mg, uid/qd; oral, 1 mg, bid, oral; 3 mg,uid/qd; oral
Administration route: Oral
Indication: Renal Transplant
Start date: 2006-04-22
Other drugs received by patient: Ganciclovir; Clotrimazole; Magnesium Oxide (Magnesium Oxide); Lopressor; Mycelex; Bactrim; Protonix; Valganciclovir HCL; Zosyn; Vancomycin Hydrochloride; Novolin N; Vytorin; Flomax (Morniflumate); Aspirin; Vicodin; Lexapro; Furosemide; Fosamax; Isosorbide Mononitrate; Allopurinol; Colchicum JTL LIQ; Potassium Chloride; Multivitamin; Rapamune; Insulin; Heparin; Cefazolin; Ciprofloxacin; Metronidazole; Oxycodone HCL; Tamsulosin Hydrochloride (Tamsulosin Hydrochloride); Insulin Suspension, NPH (Insulin Injection,isophane)
Adverse event in female receiving Prednisone
Reported by a physician from Italy on 2007-10-31
Patient: female
Adverse reactions / side effects: Psychomotor Hyperactivity, Sensory Disturbance, Depressed Level of Consciousness, Cognitive Disorder
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Bortezomib
Indication: Drug USE FOR Unknown Indication
Fentanyl
Indication: Drug USE FOR Unknown Indication
Melphalan
Indication: Drug USE FOR Unknown Indication
Prednisone
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Lansoprazole; Vaseretic; Aspirin; Plasil
Adverse event in 64 year old female receiving Prednisone
Reported by a consumer/non-health professional from United States on 2007-10-31
Patient: 64 year old female
Adverse reactions / side effects: Condition Aggravated
Suspect drug(s):
Combivent
Indication: Asthma
Prednisone
Other drugs received by patient: Allegra; Oxygen
Adverse event in 54 year old male receiving Prednisone
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-30
Patient: 54 year old male
Adverse reactions / side effects: Pulmonary Embolism
Adverse event resulted in: hospitalization
Suspect drug(s):
Fluconazole
Dosage: 200 mg
Indication: Pneumonia Cryptococcal
Start date: 2007-03-29
Mycophenolate Mofetil
Dosage: 500 mg, bid, oral
Administration route: Oral
Indication: Liver Transplant
Start date: 2006-11-08
Prednisone
Dosage: 2.5 mg, uid/qd, oral
Administration route: Oral
Indication: Liver Transplant
Start date: 2006-09-13
Prograf
Dosage: 0.5 mg, bid, oral
Administration route: Oral
Indication: Liver Transplant
Start date: 2006-09-13
Other drugs received by patient: Protonix; Actigall; Magnesium Oxide (Magnesium Oxide); Calcium with Vitamin D (Ergocalciferol, Calcium Sodium Lactate, Calciu; Actonel
Adverse event in 62 year old female receiving Prednisone
Reported by a individual with unspecified qualification from United Kingdom on 2007-10-30
Patient: 62 year old female
Adverse reactions / side effects: Viral Infection, JC Virus Infection, Muscle Twitching, Progressive Multifocal Leukoencephalopathy
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Cyclophosphamide
Indication: Chronic Lymphocytic Leukaemia
Start date: 2003-09-01
End date: 2004-02-01
Doxorubicin Hydrochloride
Indication: Chronic Lymphocytic Leukaemia
Start date: 2003-09-01
End date: 2004-02-01
Prednisone
Indication: Chronic Lymphocytic Leukaemia
Start date: 2003-09-01
End date: 2004-02-01
Rituximab
Indication: Chronic Lymphocytic Leukaemia
Start date: 2003-09-01
End date: 2006-02-01
Vincristine
Indication: Chronic Lymphocytic Leukaemia
Start date: 2003-09-01
End date: 2004-02-01
Other drugs received by patient: Chlorambucil; Fludarabine Phosphate
Adverse event in 40 year old male receiving Prednisone
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-29
Patient: 40 year old male
Adverse reactions / side effects: Proteinuria, Focal Glomerulosclerosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Methylprednisolone
Dosage: 500 mg, iv drip
Indication: Prophylaxis Against Transplant Rejection
Start date: 2005-08-04
Mycophenolate Mofetil
Dosage: 500 mg, bid, oral
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2005-08-04
Prednisone
Dosage: 5 mg, oral
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2005-08-10
Prograf
Dosage: 2 mg, bid, oral
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2005-08-05
Other drugs received by patient: Zoloft; Aciphex; Septra; Valganciclovir HCL; Protonix; Colace (Docusate Sodium); Metoprolol Tartrate; Synthroid; Magnesium Oxide (Magnesium Oxide)
Adverse event in female receiving Prednisone
Reported by a consumer/non-health professional from United States on 2007-10-29
Patient: female, weighing 77.0 kg (169.4 pounds)
Adverse reactions / side effects: Myalgia, Bedridden, Erythema Infectiosum, Fatigue, Arthralgia, Drug Ineffective, Hernia Repair, Asthenia, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Caduet
Administration route: Oral
Indication: Hypertension
Caduet
Indication: Blood Cholesterol Increased
Celebrex
Indication: Arthralgia
Start date: 2007-01-01
End date: 2007-01-01
Prednisone
Dosage: text:10 to 40mg daily
Indication: Erythema Infectiosum
Start date: 2007-01-01
End date: 2007-01-01
Other drugs received by patient: Antihypertensives
Adverse event in 67 year old male receiving Prednisone
Reported by a physician from United States on 2007-10-29
Patient: 67 year old male, weighing 77.9 kg (171.4 pounds)
Adverse reactions / side effects: Multiple Myeloma
Adverse event resulted in: death, hospitalization, disablity
Suspect drug(s):
Mycophenolate Mofetil
Administration route: Oral
Start date: 2005-12-13
Prednisone
Administration route: Oral
Start date: 2005-12-30
Tacrolimus
Dosage: therapy reported as 4mg at 9 am and 5 mg at 9 pm.
Administration route: Oral
Start date: 2006-02-08
Other drugs received by patient: Insulin; Calcium Carbonate; Allopurinol; Zocor; Hydrochlorothiazide; Rocaltrol; Heparin; Felodipine; Lopressor; Metoprolol; Lantus; Clonidine; Zosyn; Hydralazine HCL; MG Oxide; Reglan; Aspirin; 1 Concomitant Drug
Adverse event in 71 year old male receiving Prednisone
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-29
Patient: 71 year old male
Adverse reactions / side effects: Cellulitis, Complications of Transplanted Kidney, Arteriovenous Graft Site Infection, Graft Thrombosis, Anuria
Adverse event resulted in: hospitalization
Suspect drug(s):
Daclizumab(daclizumab)
Dosage: 136 mg, total dose, iv nos
Indication: Prophylaxis Against Transplant Rejection
Start date: 2004-12-05
End date: 2004-12-05
Mycophenolate Mofetil
Dosage: 1000 mg, bid, oral; 750 mg, bid, oral
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2004-12-05
Prednisone
Dosage: 10 mg, uid/qd, oral
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2004-12-07
Prograf
Dosage: 10 mg, uid/qd, oral
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2004-12-05
Other drugs received by patient: Lasix (Furosemide, Furosemide Sodium); Bactrim; Pepcid; Aspirin; Flomax; Pravachol; Actonel; Synthroid; Trazodone (Trazodone Hydrochloride); Depakote; Sinemet (Carbidopa); Ditropan; Dulcolax; Multivitamin; Mycelex
Adverse event in 75 year old male receiving Prednisone
Reported by a individual with unspecified qualification from Japan on 2007-10-29
Patient: 75 year old male
Adverse reactions / side effects: Nutritional Condition Abnormal, Pneumonia Aspiration, Rectal Haemorrhage, Clostridium Difficile Colitis, Melaena
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Adriamycin PFS
Indication: Leukaemia Plasmacytic
Cyclophosphamide
Indication: Leukaemia Plasmacytic
Dexamethasone 0.5mg TAB
Indication: Leukaemia Plasmacytic
Melphalan
Indication: Leukaemia Plasmacytic
Prednisone
Indication: Leukaemia Plasmacytic
Vincristine
Indication: Leukaemia Plasmacytic
Adverse event in male receiving Prednisone
Reported by a physician from United States on 2007-10-29
Patient: male, weighing 73.6 kg (161.9 pounds)
Adverse reactions / side effects: Atrial Fibrillation, Metabolic Encephalopathy
Adverse event resulted in: hospitalization
Suspect drug(s):
Prednisone
Indication: Prophylaxis Against Transplant Rejection
Prograf
Indication: Prophylaxis Against Transplant Rejection
End date: 2005-02-01
Prograf
Start date: 2005-02-01
Sirolimus
Administration route: Oral
Indication: Prophylaxis Against Transplant Rejection
Start date: 2005-01-31
Other drugs received by patient: Atenolol; Mycelex; Darvocet; Flonase; Theragran-M; Pravachol; Coumadin; Coumadin; Cefepime; Protonix; Flomax; Bactrim; Valcyte; Neurontin; Albuterol; Cipro; Sodium Bicarbonate; Sodium Bicarbonate; Lantus; Novolog; Amphojel; Naftin; Miralax
Adverse event in female receiving Prednisone
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: female
Adverse reactions / side effects: Dyspnoea, Vomiting, Nausea, Gastric Ulcer Haemorrhage, Atrial Fibrillation, Musculoskeletal Chest Pain, Cerebrovascular Accident, Gastric Ulcer, Cardiac Failure, Pleural Effusion, Myocardial Infarction
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Diclofenac Sodium
Indication: Drug USE FOR Unknown Indication
Humira
Indication: Drug USE FOR Unknown Indication
Start date: 2003-06-01
End date: 2004-03-01
Kineret
Indication: Rheumatoid Arthritis
Start date: 2003-04-01
End date: 2003-05-01
Prednisone
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Methotrexate; Protein A Immunoadsorption Column; Hydroxychloroquine Sulfate; Metoprolol Succinate; Furosemide; Levothyroxine Sodium; Esomeprazole Magnesium
Adverse event in female receiving Prednisone
Reported by a physician from Argentina on 2007-10-26
Patient: female, weighing 58.0 kg (127.6 pounds)
Adverse reactions / side effects: Febrile Neutropenia
Adverse event resulted in: hospitalization
Suspect drug(s):
Cyclophosphamide
Dosage: 1200 mg, unk
Indication: B-Cell Lymphoma
Start date: 2006-03-24
Doxorubicin HCL
Dosage: 80 mg, unk
Indication: B-Cell Lymphoma
Start date: 2006-03-24
Prednisone
Dosage: 200 mg, unk
Administration route: Oral
Indication: B-Cell Lymphoma
Start date: 2006-03-24
Rituximab
Dosage: 600 mg, unk
Indication: B-Cell Lymphoma
Start date: 2006-03-24
Vincristine
Dosage: 2 mg, unk
Indication: B-Cell Lymphoma
Start date: 2006-03-24
Adverse event in 7 year old female receiving Prednisone
Reported by a health professional (non-physician/pharmacist) from Greece on 2007-10-26
Patient: 7 year old female, weighing 25.0 kg (55.0 pounds)
Adverse reactions / side effects: Parvovirus Infection, Histiocytosis Haematophagic, Immunosuppression, Infection in AN Immunocompromised Host
Adverse event resulted in: death
Suspect drug(s):
Azathioprine
Cyclophosphamide
Dosage: 800 mg; 1x ; iv
Start date: 2007-04-27
End date: 2007-04-27
Cyclosporine
Dosage: 1 1x
Start date: 2007-05-02
End date: 2007-05-04
Etanercept (Etanercept)
Kineret
Dosage: 2.5 mg/kg; qd; sc
Indication: Vasculitis
Start date: 2007-04-14
End date: 2007-04-20
Methotrexate
Methylprednisolone
Dosage: 300 mg; iv
Start date: 2007-05-03
End date: 2007-05-05
Prednisone
Dosage: po
Administration route: Oral
Start date: 2001-06-20
End date: 2002-05-15
Adverse event in male receiving Prednisone
Reported by a individual with unspecified qualification from United States on 2007-10-26
Patient: male, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Syncope
Adverse event resulted in: hospitalization
Suspect drug(s):
Docetaxel
Indication: Prostate Cancer Metastatic
Start date: 2006-11-09
End date: 2007-01-31
Docetaxel
Start date: 2007-02-01
End date: 2007-06-20
Prednisone
Administration route: Oral
Indication: Prostate Cancer Metastatic
Start date: 2006-11-09
End date: 2007-06-21
Prednisone
Administration route: Oral
Start date: 2007-06-21
End date: 2007-07-19
Prednisone
Administration route: Oral
Start date: 2007-07-19
End date: 2007-09-16
Other drugs received by patient: Multivit; ALL Other Therapeutic Products; Ibuprofen; Zolpidem Tartrate; Tums; Rolaids; Claritin
Adverse event in male receiving Prednisone
Reported by a physician from United States on 2007-10-26
Patient: male, weighing 70.3 kg (154.7 pounds)
Adverse reactions / side effects: Small Intestinal Obstruction, Hodgkin's Disease
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Imuran
Administration route: Oral
Indication: Crohn's Disease
Prednisone
Administration route: Oral
Indication: Crohn's Disease
Remicade
Indication: Crohn's Disease
Other drugs received by patient: Pentasa; Vitamin CAP
Adverse event in male receiving Prednisone
Reported by a physician from Israel on 2007-10-26
Patient: male
Adverse reactions / side effects: Gangrene, Klebsiella Sepsis, Escherichia Sepsis
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Prednisone
Administration route: Oral
Indication: Immunosuppressant Drug Therapy
Sirolimus
Administration route: Oral
Indication: Immunosuppressant Drug Therapy
Tacrolimus
Administration route: Oral
Indication: Immunosuppressant Drug Therapy
Adverse event in female receiving Prednisone
Reported by a consumer/non-health professional from United States on 2007-10-26
Patient: female, weighing 74.5 kg (164.0 pounds)
Adverse reactions / side effects: Adverse Drug Reaction, Infection
Adverse event resulted in: hospitalization
Suspect drug(s):
Chantix
Administration route: Oral
Indication: EX-Smoker
Start date: 2007-09-01
End date: 2007-09-01
Prednisone
Indication: Asthma
Adverse event in 25 year old female receiving Prednisone
Reported by a individual with unspecified qualification from Australia on 2007-10-26
Patient: 25 year old female
Adverse reactions / side effects: Abdominal Pain, Pulmonary Hypertension, Placental Infarction, Coagulopathy, Placental Disorder, Tachycardia, Venous Pressure Jugular Increased, Tricuspid Valve Incompetence, Cardiomegaly, Resuscitation, Vaginal Haemorrhage, Caesarean Section, Pulmonary Oedema, Fluid Retention, Hepatic Cirrhosis, Hypotension, General Physical Health Deterioration, Renal Abscess, Gastric Haemorrhage, Respiratory Distress, Electromechanical Dissociation, Drug Exposure During Pregnancy, NO Therapeutic Response, Feeding Tube Complication, Nocardia Sepsis, Pregnancy, Injection Site Haemorrhage, Mucosal Haemorrhage, Haematemesis, Ventricular Hypertrophy, Aspiration, Pulmonary Congestion, Splenomegaly, Renal Failure Acute, Intra-Uterine Death, Foetal Movements Decreased, Hyponatraemia, Condition Aggravated, Calcinosis, Purpura, Antepartum Haemorrhage, Pulmonary Fibrosis, Sepsis, Lupus Nephritis, Bradycardia
Adverse event resulted in: death
Suspect drug(s):
Orapred
Prednisone
Adverse event in male receiving Prednisone
Reported by a physician from United States on 2007-10-26
Patient: male, weighing 99.3 kg (218.5 pounds)
Adverse reactions / side effects: Confusional State, Unresponsive TO Stimuli, Atrial Fibrillation, Disorientation, Amnesia, Convulsion
Suspect drug(s):
Acyclovir
Administration route: Oral
Indication: Antiviral Prophylaxis
Antibiotics
Dilantin
Indication: Grand MAL Convulsion
Prednisone
Administration route: Oral
Indication: Transplant Rejection
Start date: 2007-08-23
End date: 2007-08-24
Prednisone
Administration route: Oral
Start date: 2007-08-24
End date: 2007-08-25
Prednisone
Administration route: Oral
Start date: 2007-08-25
End date: 2007-08-26
Prednisone
Administration route: Oral
Start date: 2007-08-27
End date: 2007-08-29
Prednisone
Dosage: daily dose:30mg
Administration route: Oral
Start date: 2007-08-29
End date: 2007-08-29
Prednisone
Dosage: daily dose:40mg
Administration route: Oral
Solu-Medrol
Indication: Transplant Rejection
Start date: 2007-08-17
End date: 2007-08-19
Solu-Medrol
Start date: 2007-08-20
End date: 2007-08-21
Solu-Medrol
Start date: 2007-08-22
End date: 2007-08-23
Vfend
Indication: Antifungal Prophylaxis
Start date: 2007-08-15
End date: 2007-08-16
Vfend
Start date: 2007-08-16
End date: 2007-09-21
Vfend
Administration route: Oral
Start date: 2007-08-22
End date: 2007-09-02
Other drugs received by patient: Cardizem; Cardizem; Cyclosporine; ALL Other Therapeutic Products; Mycophenolate Mofetil; Metronidazole
Adverse event in 71 year old male receiving Prednisone
Reported by a consumer/non-health professional from United States on 2007-10-26
Patient: 71 year old male
Adverse reactions / side effects: Weight Decreased, Weight Increased, Drug Effect Decreased, Herpes Zoster Ophthalmic, Swelling, Abdominal Distension, Headache, Somnolence, Herpes Zoster
Suspect drug(s):
Etanercept
Indication: Rheumatoid Arthritis
Lyrica
Indication: Post Herpetic Neuralgia
Prednisone
Indication: Rheumatoid Arthritis
Other drugs received by patient: Vitamin CAP; Advil
Adverse event in female receiving Prednisone
Reported by a physician from Italy on 2007-10-26
Patient: female
Adverse reactions / side effects: Psychomotor Hyperactivity, Sensory Disturbance, Depressed Level of Consciousness, Cognitive Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Bortezomib
Indication: Drug USE FOR Unknown Indication
Fentanyl
Indication: Drug USE FOR Unknown Indication
Melphalan
Indication: Drug USE FOR Unknown Indication
Prednisone
Indication: Drug USE FOR Unknown Indication
Other drugs received by patient: Lansoprazole; Vaseretic; Aspirin; Plasil
|
