Please choose an event type to view the corresponding MedsFacts report:

DYSPNOEA ( 20 FDA reports)
PNEUMONIA ( 15 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
ASTHMA ( 9 FDA reports)
PALPITATIONS ( 8 FDA reports)
CONDITION AGGRAVATED ( 7 FDA reports)
COUGH ( 7 FDA reports)
CHEST PAIN ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
MYALGIA ( 6 FDA reports)
VISION BLURRED ( 6 FDA reports)
WEIGHT INCREASED ( 6 FDA reports)
ARTHRALGIA ( 5 FDA reports)
DEPRESSION ( 5 FDA reports)
DIZZINESS ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
HYPOXIA ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MEDICATION ERROR ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
PAIN ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
TREMOR ( 5 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CATARACT ( 4 FDA reports)
DEATH ( 4 FDA reports)
DRY MOUTH ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
NAUSEA ( 4 FDA reports)
URTICARIA ( 4 FDA reports)
ANAEMIA ( 3 FDA reports)
ANXIETY ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
CHEST DISCOMFORT ( 3 FDA reports)
CHOKING ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
DEVICE MALFUNCTION ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
HYPERTENSION ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
IMPAIRED WORK ABILITY ( 3 FDA reports)
MUSCULAR WEAKNESS ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
PULMONARY HYPERTENSION ( 3 FDA reports)
SPEECH DISORDER ( 3 FDA reports)
SYNCOPE ( 3 FDA reports)
WEIGHT DECREASED ( 3 FDA reports)
WHEEZING ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
BONE DENSITY DECREASED ( 2 FDA reports)
BRONCHOSPASM ( 2 FDA reports)
COLLAPSE OF LUNG ( 2 FDA reports)
CORONARY ARTERY DISEASE ( 2 FDA reports)
CRYING ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DIARRHOEA ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSPHAGIA ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
IRON DEFICIENCY ANAEMIA ( 2 FDA reports)
LUNG INFECTION ( 2 FDA reports)
MEDICAL DEVICE COMPLICATION ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
OSTEOPOROSIS ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PRODUCTIVE COUGH ( 2 FDA reports)
RASH ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
THROAT TIGHTNESS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINARY TRACT INFECTION ( 2 FDA reports)
VIRAL INFECTION ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
VOMITING ( 2 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 2 FDA reports)
ABDOMINAL DISTENSION ( 1 FDA reports)
ABDOMINAL HERNIA ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ADJUSTMENT DISORDER ( 1 FDA reports)
ADVERSE DRUG REACTION ( 1 FDA reports)
ADVERSE REACTION ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
AGITATION ( 1 FDA reports)
ALKALOSIS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOSMIA ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHONIA ( 1 FDA reports)
APPARENT LIFE THREATENING EVENT ( 1 FDA reports)
APTYALISM ( 1 FDA reports)
ARTERIAL RUPTURE ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ASPERGILLOSIS ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BACTERIAL INFECTION ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD BICARBONATE INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD GLUCOSE DECREASED ( 1 FDA reports)
BLOOD POTASSIUM DECREASED ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD UREA INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE NEOPLASM ( 1 FDA reports)
BRAIN NEOPLASM ( 1 FDA reports)
BREAKTHROUGH PAIN ( 1 FDA reports)
BREAST ENLARGEMENT ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 1 FDA reports)
CARDIAC FLUTTER ( 1 FDA reports)
CEREBROVASCULAR ACCIDENT ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
COLON ADENOMA ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPLEX PARTIAL SEIZURES ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CREATININE RENAL CLEARANCE DECREASED ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DEHYDRATION ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DEPENDENT PERSONALITY DISORDER ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DEVICE ADHESION ISSUE ( 1 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 1 FDA reports)
DIAPHRAGMALGIA ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISBACTERIOSIS ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTERED AT INAPPROPRIATE SITE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG DOSE OMISSION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSGRAPHIA ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
EMOTIONAL DISORDER ( 1 FDA reports)
EMPHYSEMA ( 1 FDA reports)
ENCEPHALITIS ( 1 FDA reports)
ENCEPHALOPATHY ( 1 FDA reports)
EPISTAXIS ( 1 FDA reports)
EYE IRRITATION ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
GAIT DISTURBANCE ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOSSODYNIA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
GRAND MAL CONVULSION ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMORRHAGIC OVARIAN CYST ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATORENAL FAILURE ( 1 FDA reports)
HISTOPLASMOSIS ( 1 FDA reports)
HOMICIDAL IDEATION ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERSENSITIVITY ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INCREASED VISCOSITY OF BRONCHIAL SECRETION ( 1 FDA reports)
INFECTIVE EXACERBATION OF CHRONIC OBSTRUCTIVE AIRWAYS DISEASE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE ERYTHEMA ( 1 FDA reports)
INJECTION SITE NODULE ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
IRRITABILITY ( 1 FDA reports)
JOINT STIFFNESS ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABORATORY TEST INTERFERENCE ( 1 FDA reports)
LEFT ATRIAL DILATATION ( 1 FDA reports)
LOSS OF CONSCIOUSNESS ( 1 FDA reports)
LOSS OF DREAMING ( 1 FDA reports)
LUNG DISORDER ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
MACULAR DEGENERATION ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
MENSTRUATION IRREGULAR ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MOBILITY DECREASED ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYASTHENIA GRAVIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
NASAL DISORDER ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NO THERAPEUTIC RESPONSE ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
OROPHARYNGEAL PAIN ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
OROPHARYNGITIS FUNGAL ( 1 FDA reports)
OSTEOARTHRITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
OVARIAN CYST ( 1 FDA reports)
OVARIAN MASS ( 1 FDA reports)
PAIN IN EXTREMITY ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANIC ATTACK ( 1 FDA reports)
PANNICULITIS ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PATELLOFEMORAL PAIN SYNDROME ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PERICARDIAL EFFUSION ( 1 FDA reports)
PHARYNGEAL HAEMORRHAGE ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGITIS ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PYREXIA ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RED CELL DISTRIBUTION WIDTH INCREASED ( 1 FDA reports)
RESORPTION BONE INCREASED ( 1 FDA reports)
RESPIRATORY ARREST ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY DISTRESS ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SELF MUTILATION ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS HEADACHE ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SPINAL FUSION SURGERY ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
TYPE III IMMUNE COMPLEX MEDIATED REACTION ( 1 FDA reports)
ULCER HAEMORRHAGE ( 1 FDA reports)
UNDERDOSE ( 1 FDA reports)
UTERINE POLYP ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VULVAL DISORDER ( 1 FDA reports)

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