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

DRUG INEFFECTIVE ( 148 FDA reports)
DYSPNOEA ( 137 FDA reports)
DYSGEUSIA ( 55 FDA reports)
DIZZINESS ( 41 FDA reports)
COUGH ( 36 FDA reports)
PNEUMONIA ( 34 FDA reports)
DRY MOUTH ( 32 FDA reports)
NAUSEA ( 32 FDA reports)
RASH ( 25 FDA reports)
THROAT IRRITATION ( 25 FDA reports)
FATIGUE ( 23 FDA reports)
OROPHARYNGEAL PAIN ( 23 FDA reports)
HYPERSENSITIVITY ( 22 FDA reports)
FEELING ABNORMAL ( 21 FDA reports)
INSOMNIA ( 21 FDA reports)
HYPERHIDROSIS ( 20 FDA reports)
DRUG EFFECT DECREASED ( 19 FDA reports)
DYSPHONIA ( 19 FDA reports)
ASTHMA ( 18 FDA reports)
CHEST DISCOMFORT ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
ADVERSE DRUG REACTION ( 17 FDA reports)
GLOSSODYNIA ( 16 FDA reports)
TREMOR ( 16 FDA reports)
URTICARIA ( 16 FDA reports)
VISION BLURRED ( 16 FDA reports)
ASTHENIA ( 15 FDA reports)
BRONCHITIS ( 15 FDA reports)
PRODUCTIVE COUGH ( 15 FDA reports)
WHEEZING ( 14 FDA reports)
ANAPHYLACTIC REACTION ( 13 FDA reports)
DYSPNOEA EXERTIONAL ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
HEADACHE ( 13 FDA reports)
HEAT RASH ( 13 FDA reports)
RASH PRURITIC ( 13 FDA reports)
WEIGHT DECREASED ( 13 FDA reports)
BACK PAIN ( 12 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 12 FDA reports)
DEATH ( 12 FDA reports)
DECREASED APPETITE ( 12 FDA reports)
PALPITATIONS ( 12 FDA reports)
ALOPECIA ( 11 FDA reports)
APHONIA ( 11 FDA reports)
CHEST PAIN ( 11 FDA reports)
MALAISE ( 11 FDA reports)
PAIN ( 11 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 11 FDA reports)
BLOOD GLUCOSE INCREASED ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 9 FDA reports)
DIARRHOEA ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
MUSCULAR WEAKNESS ( 9 FDA reports)
NEUROPATHY PERIPHERAL ( 9 FDA reports)
PERONEAL NERVE PALSY ( 9 FDA reports)
TONGUE COATED ( 9 FDA reports)
BREATH ALCOHOL TEST POSITIVE ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CONTUSION ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
HEAD DISCOMFORT ( 8 FDA reports)
HYPOAESTHESIA ( 8 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 8 FDA reports)
RETCHING ( 8 FDA reports)
SKIN DISCOLOURATION ( 8 FDA reports)
SWELLING FACE ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
CONVULSION ( 7 FDA reports)
DRY EYE ( 7 FDA reports)
ERYTHEMA ( 7 FDA reports)
HOT FLUSH ( 7 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
STRESS ( 7 FDA reports)
THROAT TIGHTNESS ( 7 FDA reports)
VOMITING ( 7 FDA reports)
AMNESIA ( 6 FDA reports)
BIPOLAR DISORDER ( 6 FDA reports)
BLOOD SODIUM DECREASED ( 6 FDA reports)
CLUMSINESS ( 6 FDA reports)
COORDINATION ABNORMAL ( 6 FDA reports)
DELUSION ( 6 FDA reports)
DEPRESSED MOOD ( 6 FDA reports)
HEART RATE INCREASED ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
LUNG DISORDER ( 6 FDA reports)
LUNG INFECTION ( 6 FDA reports)
MANIA ( 6 FDA reports)
MELAENA ( 6 FDA reports)
MONOPLEGIA ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
SUDDEN ONSET OF SLEEP ( 6 FDA reports)
ATRIAL FIBRILLATION ( 5 FDA reports)
CHOKING ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
GLAUCOMA ( 5 FDA reports)
HEART RATE IRREGULAR ( 5 FDA reports)
INFECTION ( 5 FDA reports)
LIP PAIN ( 5 FDA reports)
NASAL CONGESTION ( 5 FDA reports)
ORAL DISCOMFORT ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PHARYNGEAL ERYTHEMA ( 5 FDA reports)
PHARYNGEAL OEDEMA ( 5 FDA reports)
PRODUCT QUALITY ISSUE ( 5 FDA reports)
PULMONARY OEDEMA ( 5 FDA reports)
SPEECH DISORDER ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
URINARY RETENTION ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
CHILLS ( 4 FDA reports)
CONSTIPATION ( 4 FDA reports)
DELIRIUM ( 4 FDA reports)
DENTAL CARIES ( 4 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 4 FDA reports)
HYPOTHYROIDISM ( 4 FDA reports)
INCORRECT DOSE ADMINISTERED ( 4 FDA reports)
INFLAMMATION ( 4 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 4 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
MEDICATION ERROR ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MUSCULOSKELETAL PAIN ( 4 FDA reports)
NECK PAIN ( 4 FDA reports)
NIGHT SWEATS ( 4 FDA reports)
OEDEMA ( 4 FDA reports)
ORAL PAIN ( 4 FDA reports)
OROPHARYNGEAL BLISTERING ( 4 FDA reports)
PAIN IN EXTREMITY ( 4 FDA reports)
PANIC ATTACK ( 4 FDA reports)
PARAESTHESIA ( 4 FDA reports)
POLLAKIURIA ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RESPIRATORY DISTRESS ( 4 FDA reports)
RESPIRATORY TRACT INFECTION ( 4 FDA reports)
RHINORRHOEA ( 4 FDA reports)
STOMATITIS ( 4 FDA reports)
THERAPY REGIMEN CHANGED ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VIRAL INFECTION ( 4 FDA reports)
ANXIETY ( 3 FDA reports)
BLOOD URIC ACID INCREASED ( 3 FDA reports)
BRONCHIAL IRRITATION ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DRY THROAT ( 3 FDA reports)
DYSPHAGIA ( 3 FDA reports)
EYE DISORDER ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEAR ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
NASOPHARYNGITIS ( 3 FDA reports)
PAROSMIA ( 3 FDA reports)
PULMONARY EMBOLISM ( 3 FDA reports)
PYREXIA ( 3 FDA reports)
SENSATION OF FOREIGN BODY ( 3 FDA reports)
SINUSITIS ( 3 FDA reports)
TACHYCARDIA ( 3 FDA reports)
TOOTH EROSION ( 3 FDA reports)
URINARY TRACT INFECTION ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ADVERSE REACTION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANGIOEDEMA ( 2 FDA reports)
ARTHRALGIA ( 2 FDA reports)
BALANCE DISORDER ( 2 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 2 FDA reports)
BLADDER OUTLET OBSTRUCTION ( 2 FDA reports)
BLINDNESS ( 2 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 2 FDA reports)
BLOOD PRESSURE INCREASED ( 2 FDA reports)
BREATH ODOUR ( 2 FDA reports)
BRONCHIECTASIS ( 2 FDA reports)
CARDIAC DISORDER ( 2 FDA reports)
CHOKING SENSATION ( 2 FDA reports)
CLAUSTROPHOBIA ( 2 FDA reports)
CONJUNCTIVITIS ALLERGIC ( 2 FDA reports)
DECREASED BRONCHIAL SECRETION ( 2 FDA reports)
DIPLOPIA ( 2 FDA reports)
DISEASE PROGRESSION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
DRUG INTOLERANCE ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DUPUYTREN'S CONTRACTURE ( 2 FDA reports)
DYSKINESIA ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
ERYTHEMA OF EYELID ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
FAECAL INCONTINENCE ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUSHING ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROINTESTINAL FUNGAL INFECTION ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HAEMOGLOBIN DECREASED ( 2 FDA reports)
HAEMOPTYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HEARING IMPAIRED ( 2 FDA reports)
HERPES SIMPLEX ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 2 FDA reports)
JC VIRUS INFECTION ( 2 FDA reports)
JC VIRUS TEST POSITIVE ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOSS OF CONSCIOUSNESS ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION FUNGAL ( 2 FDA reports)
LUMBAR RADICULOPATHY ( 2 FDA reports)
LUNG NEOPLASM MALIGNANT ( 2 FDA reports)
MULTIPLE ALLERGIES ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NONSPECIFIC REACTION ( 2 FDA reports)
NOREPINEPHRINE INCREASED ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
ORAL FUNGAL INFECTION ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PARADOXICAL DRUG REACTION ( 2 FDA reports)
PHARYNGEAL DISORDER ( 2 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 2 FDA reports)
PLEURITIC PAIN ( 2 FDA reports)
PRODUCT TASTE ABNORMAL ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PULMONARY CONGESTION ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RESPIRATORY FAILURE ( 2 FDA reports)
RHINITIS ALLERGIC ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
SLEEP APNOEA SYNDROME ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
SPONDYLOLYSIS ( 2 FDA reports)
TENDON RUPTURE ( 2 FDA reports)
THERAPEUTIC REACTION TIME DECREASED ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TOOTH MALFORMATION ( 2 FDA reports)
TOOTHACHE ( 2 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 2 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
URINE AMPHETAMINE POSITIVE ( 2 FDA reports)
VERTEBRAL INJURY ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ACNE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ANAL HAEMORRHAGE ( 1 FDA reports)
ANGER ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
AORTIC VALVE DISEASE ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
BACK DISORDER ( 1 FDA reports)
BENIGN TUMOUR EXCISION ( 1 FDA reports)
BLOOD ALCOHOL INCREASED ( 1 FDA reports)
BLOOD CHOLESTEROL ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE DECREASED ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
COCCIDIOIDOMYCOSIS ( 1 FDA reports)
COLITIS ISCHAEMIC ( 1 FDA reports)
COLON CANCER ( 1 FDA reports)
COMPRESSION FRACTURE ( 1 FDA reports)
CORNEAL DISORDER ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYANOSIS ( 1 FDA reports)
DEAFNESS ( 1 FDA reports)
DEVICE LEAKAGE ( 1 FDA reports)
DEVICE MALFUNCTION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DRUG DISPENSING ERROR ( 1 FDA reports)
DYSARTHRIA ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FEELING HOT ( 1 FDA reports)
FLATULENCE ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL DISORDER ( 1 FDA reports)
GOUT ( 1 FDA reports)
GRANULOCYTOSIS ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEART VALVE INCOMPETENCE ( 1 FDA reports)
HEPATIC FAILURE ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOKINESIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
IDIOPATHIC PULMONARY FIBROSIS ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
INCISION SITE HAEMORRHAGE ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INTERCEPTED DRUG DISPENSING ERROR ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LACERATION ( 1 FDA reports)
LEGIONELLA INFECTION ( 1 FDA reports)
LIP BLISTER ( 1 FDA reports)
LIPOATROPHY ( 1 FDA reports)
LUNG ABSCESS ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL DISCOLOURATION ( 1 FDA reports)
NASAL DISCOMFORT ( 1 FDA reports)
NO ADVERSE EVENT ( 1 FDA reports)
NON-SMALL CELL LUNG CANCER ( 1 FDA reports)
OESOPHAGEAL STENOSIS ( 1 FDA reports)
OESOPHAGEAL ULCER HAEMORRHAGE ( 1 FDA reports)
OPEN ANGLE GLAUCOMA ( 1 FDA reports)
ORAL PRURITUS ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PEAK EXPIRATORY FLOW RATE DECREASED ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
PROSTATOMEGALY ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 1 FDA reports)
RENAL DISORDER ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATION ABNORMAL ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
SENSATION OF PRESSURE ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SINUS OPERATION ( 1 FDA reports)
SKIN ATROPHY ( 1 FDA reports)
SKIN CHAPPED ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN WRINKLING ( 1 FDA reports)
SOMNOLENCE ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYSTEMIC INFLAMMATORY RESPONSE SYNDROME ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TOOTH DISCOLOURATION ( 1 FDA reports)
TOOTH LOSS ( 1 FDA reports)
TUMOUR INVASION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
VESSEL PERFORATION ( 1 FDA reports)
VITAMIN D DEFICIENCY ( 1 FDA reports)

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