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

DRUG INEFFECTIVE ( 36 FDA reports)
PRODUCT QUALITY ISSUE ( 23 FDA reports)
DYSPNOEA ( 21 FDA reports)
DIARRHOEA ( 14 FDA reports)
FATIGUE ( 14 FDA reports)
COUGH ( 13 FDA reports)
ILL-DEFINED DISORDER ( 13 FDA reports)
TREMOR ( 13 FDA reports)
NAUSEA ( 12 FDA reports)
WEIGHT INCREASED ( 12 FDA reports)
FEELING ABNORMAL ( 11 FDA reports)
HEADACHE ( 11 FDA reports)
DIZZINESS ( 10 FDA reports)
FALL ( 10 FDA reports)
ASTHMA ( 9 FDA reports)
MEDICATION ERROR ( 9 FDA reports)
ABNORMAL FAECES ( 8 FDA reports)
DRUG ADMINISTRATION ERROR ( 8 FDA reports)
DYSGEUSIA ( 8 FDA reports)
EPISTAXIS ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
GASTROINTESTINAL DISORDER ( 8 FDA reports)
INTENTIONAL DRUG MISUSE ( 8 FDA reports)
MALAISE ( 8 FDA reports)
ACCIDENT ( 7 FDA reports)
ADVERSE EVENT ( 7 FDA reports)
DEFAECATION URGENCY ( 7 FDA reports)
DYSPHONIA ( 7 FDA reports)
FOOD CRAVING ( 7 FDA reports)
HIP FRACTURE ( 7 FDA reports)
HORMONE LEVEL ABNORMAL ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
HUNGER ( 7 FDA reports)
LIMB INJURY ( 7 FDA reports)
NASOPHARYNGITIS ( 7 FDA reports)
RASH ( 7 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 7 FDA reports)
WEIGHT FLUCTUATION ( 7 FDA reports)
BURNING SENSATION ( 6 FDA reports)
MIDDLE INSOMNIA ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
CHEST PAIN ( 5 FDA reports)
HYPERKERATOSIS ( 5 FDA reports)
NERVE COMPRESSION ( 5 FDA reports)
PAIN IN EXTREMITY ( 5 FDA reports)
PNEUMONIA ( 5 FDA reports)
SENSORY LOSS ( 5 FDA reports)
TREATMENT NONCOMPLIANCE ( 5 FDA reports)
APHONIA ( 4 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
DEPRESSION ( 4 FDA reports)
INHALATION THERAPY ( 4 FDA reports)
INSOMNIA ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
PAIN ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SYNCOPE ( 4 FDA reports)
VISION BLURRED ( 4 FDA reports)
AGITATION ( 3 FDA reports)
ASTHENIA ( 3 FDA reports)
BACK PAIN ( 3 FDA reports)
BALANCE DISORDER ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CATARACT ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
EATING DISORDER ( 3 FDA reports)
IRRITABILITY ( 3 FDA reports)
MACULAR DEGENERATION ( 3 FDA reports)
MYALGIA ( 3 FDA reports)
PARTIAL SEIZURES ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
PRURITUS ( 3 FDA reports)
THROAT IRRITATION ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
AKATHISIA ( 2 FDA reports)
ANAEMIA ( 2 FDA reports)
ANXIETY ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BEDRIDDEN ( 2 FDA reports)
BLOOD GLUCOSE INCREASED ( 2 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHAPPED LIPS ( 2 FDA reports)
CHILLS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DIVERTICULITIS ( 2 FDA reports)
DRY EYE ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
FAECES DISCOLOURED ( 2 FDA reports)
HAEMATOCHEZIA ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HYPERPHAGIA ( 2 FDA reports)
HYPOTENSION ( 2 FDA reports)
HYPOTHYROIDISM ( 2 FDA reports)
NASAL DISCOMFORT ( 2 FDA reports)
OFF LABEL USE ( 2 FDA reports)
ORAL CANDIDIASIS ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PARAESTHESIA ( 2 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY DISORDER ( 2 FDA reports)
SINUSITIS ( 2 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
ABDOMINAL DISCOMFORT ( 1 FDA reports)
ABDOMINAL PAIN ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL EXPOSURE ( 1 FDA reports)
ARTERIAL OCCLUSIVE DISEASE ( 1 FDA reports)
ASTHENOPIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
ATRIAL FLUTTER ( 1 FDA reports)
AUTOIMMUNE DISORDER ( 1 FDA reports)
BLEPHAROSPASM ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 1 FDA reports)
BONE DENSITY DECREASED ( 1 FDA reports)
BREAST SWELLING ( 1 FDA reports)
BREAST TENDERNESS ( 1 FDA reports)
BRONCHITIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC FAILURE CHRONIC ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 1 FDA reports)
CONDITION AGGRAVATED ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
CRYING ( 1 FDA reports)
DENTAL CARIES ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DISABILITY ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
ENAMEL ANOMALY ( 1 FDA reports)
ENTERITIS ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
HAEMATURIA ( 1 FDA reports)
HAEMOGLOBIN DECREASED ( 1 FDA reports)
HAEMORRHAGE URINARY TRACT ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART RATE INCREASED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
KERATOPATHY ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
MALNUTRITION ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MIDDLE EAR EFFUSION ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE SPASMS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NECROTISING ULCERATIVE GINGIVOSTOMATITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NIPPLE PAIN ( 1 FDA reports)
NON-CARDIAC CHEST PAIN ( 1 FDA reports)
OEDEMA PERIPHERAL ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PALPITATIONS ( 1 FDA reports)
PHARYNGEAL ERYTHEMA ( 1 FDA reports)
PHARYNGEAL OEDEMA ( 1 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RASH VESICULAR ( 1 FDA reports)
RECTAL DISCHARGE ( 1 FDA reports)
RED BLOOD CELL SEDIMENTATION RATE INCREASED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RESTLESSNESS ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SENSATION OF BLOOD FLOW ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN INDURATION ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SPUTUM DISCOLOURED ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STOMACH DISCOMFORT ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROMBOCYTHAEMIA ( 1 FDA reports)
TONGUE COATED ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
VERTIGO ( 1 FDA reports)
VISUAL DISTURBANCE ( 1 FDA reports)
VOMITING ( 1 FDA reports)
WITHDRAWAL SYNDROME ( 1 FDA reports)

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