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

NAUSEA ( 63 FDA reports)
DRUG INEFFECTIVE ( 57 FDA reports)
PAIN ( 53 FDA reports)
DYSPNOEA ( 49 FDA reports)
VOMITING ( 45 FDA reports)
HEADACHE ( 44 FDA reports)
FATIGUE ( 37 FDA reports)
FEELING ABNORMAL ( 35 FDA reports)
SOMNOLENCE ( 34 FDA reports)
DIZZINESS ( 32 FDA reports)
ASTHENIA ( 31 FDA reports)
PNEUMONIA ( 31 FDA reports)
PRODUCT QUALITY ISSUE ( 30 FDA reports)
INSOMNIA ( 29 FDA reports)
SUICIDAL IDEATION ( 29 FDA reports)
ABDOMINAL PAIN UPPER ( 26 FDA reports)
PULMONARY EMBOLISM ( 25 FDA reports)
WEIGHT INCREASED ( 25 FDA reports)
CONSTIPATION ( 24 FDA reports)
TREMOR ( 24 FDA reports)
DEPRESSION ( 23 FDA reports)
DISTURBANCE IN ATTENTION ( 23 FDA reports)
LOSS OF CONSCIOUSNESS ( 23 FDA reports)
MALAISE ( 23 FDA reports)
BLOOD GLUCOSE INCREASED ( 22 FDA reports)
INJURY ( 22 FDA reports)
MYALGIA ( 22 FDA reports)
EATING DISORDER ( 21 FDA reports)
HYPOTENSION ( 21 FDA reports)
PARAESTHESIA ( 21 FDA reports)
MEMORY IMPAIRMENT ( 20 FDA reports)
MUSCLE SPASMS ( 20 FDA reports)
CRYING ( 19 FDA reports)
DRY EYE ( 19 FDA reports)
EYE DISORDER ( 19 FDA reports)
WEIGHT DECREASED ( 19 FDA reports)
ASTHMA ( 18 FDA reports)
DIARRHOEA ( 18 FDA reports)
PRURITUS ( 18 FDA reports)
PAIN IN EXTREMITY ( 17 FDA reports)
AGGRESSION ( 16 FDA reports)
ANXIETY ( 16 FDA reports)
ARTHRALGIA ( 16 FDA reports)
COUGH ( 16 FDA reports)
PYREXIA ( 16 FDA reports)
ABASIA ( 15 FDA reports)
AMNESIA ( 15 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 15 FDA reports)
FLUSHING ( 15 FDA reports)
INFECTION ( 15 FDA reports)
OEDEMA PERIPHERAL ( 15 FDA reports)
RASH ( 15 FDA reports)
VISUAL ACUITY REDUCED ( 15 FDA reports)
ABNORMAL DREAMS ( 14 FDA reports)
BALANCE DISORDER ( 14 FDA reports)
CHEST PAIN ( 14 FDA reports)
CONVULSION ( 14 FDA reports)
DYSPHAGIA ( 14 FDA reports)
HYPOXIA ( 14 FDA reports)
MYOCARDIAL INFARCTION ( 14 FDA reports)
OFF LABEL USE ( 14 FDA reports)
PULMONARY OEDEMA ( 14 FDA reports)
URTICARIA ( 14 FDA reports)
ABDOMINAL DISTENSION ( 13 FDA reports)
ALOPECIA ( 13 FDA reports)
DECREASED APPETITE ( 13 FDA reports)
FALL ( 13 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
HYPOAESTHESIA ( 13 FDA reports)
IRRITABILITY ( 13 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 12 FDA reports)
APNOEA ( 12 FDA reports)
COLLAPSE OF LUNG ( 12 FDA reports)
DEPRESSED MOOD ( 12 FDA reports)
DRUG ADMINISTRATION ERROR ( 12 FDA reports)
EMOTIONAL DISTRESS ( 12 FDA reports)
HYPERSENSITIVITY ( 12 FDA reports)
IMMUNOGLOBULINS DECREASED ( 12 FDA reports)
INTESTINAL PERFORATION ( 12 FDA reports)
LUNG INJURY ( 12 FDA reports)
PREMATURE BABY ( 12 FDA reports)
RESPIRATORY DISORDER ( 12 FDA reports)
RESPIRATORY DISTRESS ( 12 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 12 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 12 FDA reports)
BLOOD PRESSURE DECREASED ( 11 FDA reports)
BLOOD PRESSURE INCREASED ( 11 FDA reports)
CONFUSIONAL STATE ( 11 FDA reports)
HEAD INJURY ( 11 FDA reports)
RESTLESSNESS ( 11 FDA reports)
BLOOD POTASSIUM DECREASED ( 10 FDA reports)
CEREBROVASCULAR ACCIDENT ( 10 FDA reports)
DRUG INTERACTION ( 10 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 10 FDA reports)
HYPERHIDROSIS ( 10 FDA reports)
HYPERTONIC BLADDER ( 10 FDA reports)
IMPAIRED WORK ABILITY ( 10 FDA reports)
INJECTION SITE ERYTHEMA ( 10 FDA reports)
MOOD SWINGS ( 10 FDA reports)
PANIC ATTACK ( 10 FDA reports)
PHOTOSENSITIVITY REACTION ( 10 FDA reports)
SUICIDE ATTEMPT ( 10 FDA reports)
BACK PAIN ( 9 FDA reports)
CHOLECYSTITIS CHRONIC ( 9 FDA reports)
CONTUSION ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 9 FDA reports)
DRUG HYPERSENSITIVITY ( 9 FDA reports)
DRY MOUTH ( 9 FDA reports)
GASTRIC DISORDER ( 9 FDA reports)
MENTAL DISORDER ( 9 FDA reports)
SYNCOPE ( 9 FDA reports)
VISION BLURRED ( 9 FDA reports)
ABDOMINAL PAIN ( 8 FDA reports)
ANGER ( 8 FDA reports)
BIPOLAR DISORDER ( 8 FDA reports)
CONDITION AGGRAVATED ( 8 FDA reports)
DISORIENTATION ( 8 FDA reports)
DRUG EFFECT DECREASED ( 8 FDA reports)
EMOTIONAL DISORDER ( 8 FDA reports)
FEELING HOT ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
HYPERPHAGIA ( 8 FDA reports)
IMPAIRED DRIVING ABILITY ( 8 FDA reports)
INCORRECT DOSE ADMINISTERED ( 8 FDA reports)
MENTAL IMPAIRMENT ( 8 FDA reports)
NASOPHARYNGITIS ( 8 FDA reports)
NERVOUS SYSTEM DISORDER ( 8 FDA reports)
NIGHTMARE ( 8 FDA reports)
OVERDOSE ( 8 FDA reports)
PULMONARY VALVE STENOSIS ( 8 FDA reports)
RESTLESS LEGS SYNDROME ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
BURNING SENSATION ( 7 FDA reports)
CHOLELITHIASIS ( 7 FDA reports)
COGNITIVE DISORDER ( 7 FDA reports)
DRUG DOSE OMISSION ( 7 FDA reports)
DYSARTHRIA ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
EYELID FUNCTION DISORDER ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
INJECTION SITE BRUISING ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INJECTION SITE REACTION ( 7 FDA reports)
LIBIDO DECREASED ( 7 FDA reports)
LYMPHADENOPATHY ( 7 FDA reports)
MENINGITIS ( 7 FDA reports)
MIGRAINE ( 7 FDA reports)
MUSCLE DISORDER ( 7 FDA reports)
NO ADVERSE EVENT ( 7 FDA reports)
PLEURITIC PAIN ( 7 FDA reports)
PULMONARY INFARCTION ( 7 FDA reports)
SINUSITIS ( 7 FDA reports)
SKIN DISCOLOURATION ( 7 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 6 FDA reports)
CHILLS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
CYANOSIS ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 6 FDA reports)
DYSKINESIA ( 6 FDA reports)
DYSPHONIA ( 6 FDA reports)
EYE SWELLING ( 6 FDA reports)
GALLBLADDER DISORDER ( 6 FDA reports)
GALLBLADDER INJURY ( 6 FDA reports)
HEPATIC STEATOSIS ( 6 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 6 FDA reports)
INJECTION SITE URTICARIA ( 6 FDA reports)
NEURALGIA ( 6 FDA reports)
PALPITATIONS ( 6 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 6 FDA reports)
PHARYNGEAL OEDEMA ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
PULMONARY THROMBOSIS ( 6 FDA reports)
RASH GENERALISED ( 6 FDA reports)
RASH MACULAR ( 6 FDA reports)
RETCHING ( 6 FDA reports)
RHINITIS ALLERGIC ( 6 FDA reports)
SENSORY LOSS ( 6 FDA reports)
UROSEPSIS ( 6 FDA reports)
WHEEZING ( 6 FDA reports)
ABNORMAL BEHAVIOUR ( 5 FDA reports)
ABSCESS LIMB ( 5 FDA reports)
ANAEMIA ( 5 FDA reports)
ANOREXIA ( 5 FDA reports)
APHASIA ( 5 FDA reports)
BILIARY DYSKINESIA ( 5 FDA reports)
BLOOD PHOSPHORUS DECREASED ( 5 FDA reports)
BONE PAIN ( 5 FDA reports)
CHOKING SENSATION ( 5 FDA reports)
DROOLING ( 5 FDA reports)
DYSURIA ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
EMPHYSEMA ( 5 FDA reports)
ERECTILE DYSFUNCTION ( 5 FDA reports)
EYE IRRITATION ( 5 FDA reports)
HALLUCINATION, AUDITORY ( 5 FDA reports)
HEART RATE INCREASED ( 5 FDA reports)
HYPOACUSIS ( 5 FDA reports)
ILL-DEFINED DISORDER ( 5 FDA reports)
INJECTION SITE HAEMORRHAGE ( 5 FDA reports)
INJECTION SITE PAIN ( 5 FDA reports)
INJECTION SITE STREAKING ( 5 FDA reports)
INJECTION SITE WARMTH ( 5 FDA reports)
INTENTIONAL SELF-INJURY ( 5 FDA reports)
INTRACRANIAL HYPOTENSION ( 5 FDA reports)
IRIS DISORDER ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
OTITIS EXTERNA ( 5 FDA reports)
POST CONCUSSION SYNDROME ( 5 FDA reports)
POST LUMBAR PUNCTURE SYNDROME ( 5 FDA reports)
PYELONEPHRITIS ( 5 FDA reports)
STRESS ( 5 FDA reports)
TINNITUS ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
VISUAL IMPAIRMENT ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
AFFECT LABILITY ( 4 FDA reports)
AGEUSIA ( 4 FDA reports)
ANOSMIA ( 4 FDA reports)
APPLICATION SITE ERYTHEMA ( 4 FDA reports)
ARRHYTHMIA ( 4 FDA reports)
ATRIAL FIBRILLATION ( 4 FDA reports)
BRONCHITIS ( 4 FDA reports)
CANDIDIASIS ( 4 FDA reports)
CARDIAC ARREST ( 4 FDA reports)
CATARACT ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
CORONARY ARTERY DISEASE ( 4 FDA reports)
DRY SKIN ( 4 FDA reports)
DYSGEUSIA ( 4 FDA reports)
ERYTHEMA ( 4 FDA reports)
EUPHORIC MOOD ( 4 FDA reports)
FOOT FRACTURE ( 4 FDA reports)
GRAND MAL CONVULSION ( 4 FDA reports)
HAEMATOCHEZIA ( 4 FDA reports)
HAEMOGLOBIN DECREASED ( 4 FDA reports)
HAEMORRHAGE ( 4 FDA reports)
HALLUCINATION, VISUAL ( 4 FDA reports)
HOT FLUSH ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INTENTIONAL DRUG MISUSE ( 4 FDA reports)
ISCHAEMIC CEREBRAL INFARCTION ( 4 FDA reports)
LACRIMATION INCREASED ( 4 FDA reports)
LOWER LIMB FRACTURE ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NECK INJURY ( 4 FDA reports)
NERVOUSNESS ( 4 FDA reports)
OBSESSIVE THOUGHTS ( 4 FDA reports)
OPTIC NERVE DISORDER ( 4 FDA reports)
OROPHARYNGEAL PAIN ( 4 FDA reports)
PANCREATIC DISORDER ( 4 FDA reports)
PHARYNGOLARYNGEAL PAIN ( 4 FDA reports)
PHOTOPSIA ( 4 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 4 FDA reports)
SKIN LESION ( 4 FDA reports)
SPEECH DISORDER ( 4 FDA reports)
SWELLING FACE ( 4 FDA reports)
THINKING ABNORMAL ( 4 FDA reports)
THROAT TIGHTNESS ( 4 FDA reports)
THROMBOSIS ( 4 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
ABDOMINAL TENDERNESS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
ADVERSE DRUG REACTION ( 3 FDA reports)
ANAPHYLACTIC REACTION ( 3 FDA reports)
ANGIOPATHY ( 3 FDA reports)
ANOXIC ENCEPHALOPATHY ( 3 FDA reports)
APHONIA ( 3 FDA reports)
ARTHRITIS ( 3 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 3 FDA reports)
BACK DISORDER ( 3 FDA reports)
BLEPHAROSPASM ( 3 FDA reports)
BLISTER ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
BODY HEIGHT DECREASED ( 3 FDA reports)
BONE DISORDER ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
DEFORMITY ( 3 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 3 FDA reports)
DIFFICULTY IN WALKING ( 3 FDA reports)
DISCOMFORT ( 3 FDA reports)
DYSMENORRHOEA ( 3 FDA reports)
EPISTAXIS ( 3 FDA reports)
ERYTHEMA OF EYELID ( 3 FDA reports)
EYE MOVEMENT DISORDER ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
EYELASH DISCOLOURATION ( 3 FDA reports)
FEELING COLD ( 3 FDA reports)
FOREIGN BODY SENSATION IN EYES ( 3 FDA reports)
GROWTH OF EYELASHES ( 3 FDA reports)
HAEMATURIA ( 3 FDA reports)
HAIR TEXTURE ABNORMAL ( 3 FDA reports)
HOSPITALISATION ( 3 FDA reports)
HYPERGLYCAEMIA ( 3 FDA reports)
HYPERSOMNIA ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
INJECTION SITE HAEMATOMA ( 3 FDA reports)
INJECTION SITE PRURITUS ( 3 FDA reports)
INJECTION SITE RASH ( 3 FDA reports)
INTENTIONAL OVERDOSE ( 3 FDA reports)
JOINT SWELLING ( 3 FDA reports)
KNEE ARTHROPLASTY ( 3 FDA reports)
LACERATION ( 3 FDA reports)
LIP SWELLING ( 3 FDA reports)
LUNG HYPERINFLATION ( 3 FDA reports)
MEDICATION ERROR ( 3 FDA reports)
MENIERE'S DISEASE ( 3 FDA reports)
MENINGITIS VIRAL ( 3 FDA reports)
METRORRHAGIA ( 3 FDA reports)
MICTURITION URGENCY ( 3 FDA reports)
MUSCULOSKELETAL PAIN ( 3 FDA reports)
NASAL DISCOMFORT ( 3 FDA reports)
NERVE INJURY ( 3 FDA reports)
NEUROPATHY PERIPHERAL ( 3 FDA reports)
OLIGURIA ( 3 FDA reports)
ORAL DISCOMFORT ( 3 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 3 FDA reports)
PLATELET COUNT DECREASED ( 3 FDA reports)
PUPIL FIXED ( 3 FDA reports)
RASH PAPULAR ( 3 FDA reports)
RESPIRATORY ARREST ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SCAR ( 3 FDA reports)
SEASONAL ALLERGY ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SKIN ULCER ( 3 FDA reports)
SLEEP DISORDER ( 3 FDA reports)
SNEEZING ( 3 FDA reports)
SWOLLEN TONGUE ( 3 FDA reports)
TENDONITIS ( 3 FDA reports)
TOOTH DISORDER ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
TREATMENT NONCOMPLIANCE ( 3 FDA reports)
VAGINAL HAEMORRHAGE ( 3 FDA reports)
ABNORMAL SENSATION IN EYE ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACCIDENT ( 2 FDA reports)
ACCIDENTAL EXPOSURE ( 2 FDA reports)
ACNE ( 2 FDA reports)
ACUTE PULMONARY OEDEMA ( 2 FDA reports)
ACUTE RESPIRATORY FAILURE ( 2 FDA reports)
ADHESION ( 2 FDA reports)
ADRENAL DISORDER ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
ANORGASMIA ( 2 FDA reports)
APPLICATION SITE IRRITATION ( 2 FDA reports)
APPLICATION SITE RASH ( 2 FDA reports)
ARTERIAL DISORDER ( 2 FDA reports)
ARTHROPOD BITE ( 2 FDA reports)
ASPHYXIA ( 2 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD GLUCOSE DECREASED ( 2 FDA reports)
BODY HEIGHT INCREASED ( 2 FDA reports)
BOWEL MOVEMENT IRREGULARITY ( 2 FDA reports)
BREAST CANCER FEMALE ( 2 FDA reports)
BREAST TENDERNESS ( 2 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CARDIAC OPERATION ( 2 FDA reports)
CARDIAC PACEMAKER INSERTION ( 2 FDA reports)
CARDIAC VALVE DISEASE ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMPLETED SUICIDE ( 2 FDA reports)
COORDINATION ABNORMAL ( 2 FDA reports)
CORONARY ARTERY OCCLUSION ( 2 FDA reports)
COSTOCHONDRITIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
DELIVERY ( 2 FDA reports)
DENTAL CARIES ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DISEASE RECURRENCE ( 2 FDA reports)
DISSEMINATED INTRAVASCULAR COAGULATION ( 2 FDA reports)
DRUG DEPENDENCE ( 2 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 2 FDA reports)
DYSCALCULIA ( 2 FDA reports)
DYSGRAPHIA ( 2 FDA reports)
DYSTONIA ( 2 FDA reports)
EXPIRED DRUG ADMINISTERED ( 2 FDA reports)
EYELID OEDEMA ( 2 FDA reports)
FACE INJURY ( 2 FDA reports)
FAILURE OF IMPLANT ( 2 FDA reports)
FEMUR FRACTURE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER OPERATION ( 2 FDA reports)
GASTROENTERITIS VIRAL ( 2 FDA reports)
GASTROINTESTINAL DISORDER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL RECESSION ( 2 FDA reports)
GLOSSODYNIA ( 2 FDA reports)
HAIR GROWTH ABNORMAL ( 2 FDA reports)
HALLUCINATION ( 2 FDA reports)
HEART RATE DECREASED ( 2 FDA reports)
HEART RATE IRREGULAR ( 2 FDA reports)
HEPARIN-INDUCED THROMBOCYTOPENIA ( 2 FDA reports)
HERPES ZOSTER ( 2 FDA reports)
HIATUS HERNIA ( 2 FDA reports)
HYPERCHLORHYDRIA ( 2 FDA reports)
HYPOKINESIA ( 2 FDA reports)
IMPAIRED HEALING ( 2 FDA reports)
INCORRECT STORAGE OF DRUG ( 2 FDA reports)
INCREASED APPETITE ( 2 FDA reports)
INCREASED UPPER AIRWAY SECRETION ( 2 FDA reports)
INHALATION THERAPY ( 2 FDA reports)
INITIAL INSOMNIA ( 2 FDA reports)
INJECTION SITE DISCOLOURATION ( 2 FDA reports)
LABILE BLOOD PRESSURE ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 2 FDA reports)
LOCAL SWELLING ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
MOBILITY DECREASED ( 2 FDA reports)
MULTI-ORGAN FAILURE ( 2 FDA reports)
MULTIPLE SCLEROSIS ( 2 FDA reports)
MUSCLE ATROPHY ( 2 FDA reports)
MUSCLE RIGIDITY ( 2 FDA reports)
MUSCLE STRAIN ( 2 FDA reports)
MYCOSIS FUNGOIDES ( 2 FDA reports)
NASAL SEPTUM PERFORATION ( 2 FDA reports)
NECK PAIN ( 2 FDA reports)
NEGATIVISM ( 2 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OESOPHAGEAL SPASM ( 2 FDA reports)
ONYCHOCLASIS ( 2 FDA reports)
OPTIC ATROPHY ( 2 FDA reports)
OROMANDIBULAR DYSTONIA ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN JAW ( 2 FDA reports)
PANCREATITIS ( 2 FDA reports)
PANIC REACTION ( 2 FDA reports)
PERICARDIAL EFFUSION ( 2 FDA reports)
PERICARDITIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERIPHERAL ISCHAEMIA ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PHARYNGITIS ( 2 FDA reports)
PHARYNGOESOPHAGEAL DIVERTICULUM ( 2 FDA reports)
PLEURISY ( 2 FDA reports)
PNEUMONIA BACTERIAL ( 2 FDA reports)
PNEUMOTHORAX ( 2 FDA reports)
PRESYNCOPE ( 2 FDA reports)
PROTEIN TOTAL DECREASED ( 2 FDA reports)
PSEUDOMONAS INFECTION ( 2 FDA reports)
RENAL PAIN ( 2 FDA reports)
RESPIRATORY TRACT CONGESTION ( 2 FDA reports)
RHEUMATOID ARTHRITIS ( 2 FDA reports)
RHINALGIA ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SECRETION DISCHARGE ( 2 FDA reports)
SENSATION OF HEAVINESS ( 2 FDA reports)
SKIN DISORDER ( 2 FDA reports)
STAPHYLOCOCCAL INFECTION ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
SURGERY ( 2 FDA reports)
SWELLING ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
UPPER LIMB FRACTURE ( 2 FDA reports)
UPPER RESPIRATORY FUNGAL INFECTION ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
URINE OUTPUT DECREASED ( 2 FDA reports)
VENTRICULAR DYSFUNCTION ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VERTIGO ( 2 FDA reports)
VULVOVAGINAL DRYNESS ( 2 FDA reports)
VULVOVAGINAL PAIN ( 2 FDA reports)
WALKING AID USER ( 2 FDA reports)
WHEELCHAIR USER ( 2 FDA reports)
WOUND SECRETION ( 2 FDA reports)
ABDOMINAL PAIN LOWER ( 1 FDA reports)
ABNORMAL LOSS OF WEIGHT ( 1 FDA reports)
ACCIDENT AT WORK ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACCIDENTAL OVERDOSE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE DISSEMINATED ENCEPHALOMYELITIS ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALLERGY TEST POSITIVE ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANGIONEUROTIC OEDEMA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHAGIA ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
APLASTIC ANAEMIA ( 1 FDA reports)
APPLICATION SITE PRURITUS ( 1 FDA reports)
APPLICATION SITE SWELLING ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BACTERIA URINE ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BEDRIDDEN ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLADDER TRABECULATION ( 1 FDA reports)
BLEPHARITIS ( 1 FDA reports)
BLOOD CORTISOL ABNORMAL ( 1 FDA reports)
BLOOD COUNT ABNORMAL ( 1 FDA reports)
BLOOD CREATINE PHOSPHOKINASE MB INCREASED ( 1 FDA reports)
BLOOD CREATININE INCREASED ( 1 FDA reports)
BLOOD PRESSURE ABNORMAL ( 1 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC DECREASED ( 1 FDA reports)
BLOOD PROLACTIN INCREASED ( 1 FDA reports)
BLOOD TESTOSTERONE ABNORMAL ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BORDERLINE PERSONALITY DISORDER ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRADYPHRENIA ( 1 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BREAST DISCOMFORT ( 1 FDA reports)
BREAST PAIN ( 1 FDA reports)
BREATH SOUNDS ABNORMAL ( 1 FDA reports)
BRONCHITIS BACTERIAL ( 1 FDA reports)
BRUXISM ( 1 FDA reports)
BURSITIS ( 1 FDA reports)
CARBON DIOXIDE INCREASED ( 1 FDA reports)
CARDIAC FAILURE ( 1 FDA reports)
CARDIAC STRESS TEST NORMAL ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CAST APPLICATION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LESION ( 1 FDA reports)
CHANGE OF BOWEL HABIT ( 1 FDA reports)
CHEMICAL BURN OF GASTROINTESTINAL TRACT ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHROMATURIA ( 1 FDA reports)
CIRCULATORY COLLAPSE ( 1 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLITIS ULCERATIVE ( 1 FDA reports)
CONJUNCTIVITIS INFECTIVE ( 1 FDA reports)
CONTACT LENS INTOLERANCE ( 1 FDA reports)
CYST ( 1 FDA reports)
DANDRUFF ( 1 FDA reports)
DAYDREAMING ( 1 FDA reports)
DEATH ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEPENDENCE ON ENABLING MACHINE OR DEVICE ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DERMATITIS CONTACT ( 1 FDA reports)
DEVICE FAILURE ( 1 FDA reports)
DEVICE RELATED SEPSIS ( 1 FDA reports)
DIABETES MELLITUS INSULIN-DEPENDENT ( 1 FDA reports)
DIAPHRAGMATIC DISORDER ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG PRESCRIBING ERROR ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN NEGATIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DYSPLASIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EAR INFECTION ( 1 FDA reports)
EAR PRURITUS ( 1 FDA reports)
ECCHYMOSIS ( 1 FDA reports)
EJECTION FRACTION DECREASED ( 1 FDA reports)
ENDOCRINE DISORDER ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPRESSIVE LANGUAGE DISORDER ( 1 FDA reports)
EXTRASYSTOLES ( 1 FDA reports)
EYE ALLERGY ( 1 FDA reports)
EYE BURNS ( 1 FDA reports)
EYE DISCHARGE ( 1 FDA reports)
EYE INFECTION ( 1 FDA reports)
EYE INFLAMMATION ( 1 FDA reports)
EYELID PTOSIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEELING DRUNK ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FOOD INTOLERANCE ( 1 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GASTRIC POLYPS ( 1 FDA reports)
GASTRIC ULCER ( 1 FDA reports)
GASTRITIS HAEMORRHAGIC ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GENE MUTATION ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GINGIVAL SWELLING ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLOSSITIS ( 1 FDA reports)
GOITRE ( 1 FDA reports)
GOUT ( 1 FDA reports)
HAEMATEMESIS ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMATOMA ( 1 FDA reports)
HAEMOGLOBIN ABNORMAL ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEREDITARY ANGIOEDEMA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 1 FDA reports)
HISTOPLASMOSIS DISSEMINATED ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKERATOSIS ( 1 FDA reports)
HYPOAESTHESIA FACIAL ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPONATRAEMIA ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCORRECT ROUTE OF DRUG ADMINISTRATION ( 1 FDA reports)
INCREASED TENDENCY TO BRUISE ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INJECTION SITE BURNING ( 1 FDA reports)
INJECTION SITE EXTRAVASATION ( 1 FDA reports)
INJECTION SITE MASS ( 1 FDA reports)
INJECTION SITE SWELLING ( 1 FDA reports)
INJECTION SITE VESICLES ( 1 FDA reports)
INJURY ASPHYXIATION ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
IRITIS ( 1 FDA reports)
JAW DISORDER ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACUNAR INFARCTION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LOGORRHOEA ( 1 FDA reports)
LOSS OF EMPLOYMENT ( 1 FDA reports)
LUNG CANCER METASTATIC ( 1 FDA reports)
LUNG INFECTION ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
LYMPHANGIOMA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MANIA ( 1 FDA reports)
MEAN CELL HAEMOGLOBIN CONCENTRATION DECREASED ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
MELANOCYTIC NAEVUS ( 1 FDA reports)
MENORRHAGIA ( 1 FDA reports)
METABOLIC ACIDOSIS ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MONOPLEGIA ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOTOR DYSFUNCTION ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MUCOSAL DRYNESS ( 1 FDA reports)
MULTIPLE ALLERGIES ( 1 FDA reports)
MULTIPLE SCLEROSIS RELAPSE ( 1 FDA reports)
MUSCLE CRAMP ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL DISORDER ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOGLOBIN BLOOD DECREASED ( 1 FDA reports)
MYOSITIS ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASAL POLYPS ( 1 FDA reports)
NASAL ULCER ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NECROTISING COLITIS ( 1 FDA reports)
NEPHROLITHIASIS ( 1 FDA reports)
NEURALGIC AMYOTROPHY ( 1 FDA reports)
NUCLEAR MAGNETIC RESONANCE IMAGING BRAIN ABNORMAL ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OCCULT BLOOD POSITIVE ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
ORAL CANDIDIASIS ( 1 FDA reports)
ORAL MUCOSAL DISCOLOURATION ( 1 FDA reports)
ORAL SURGERY ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OSTEONECROSIS ( 1 FDA reports)
OVERWEIGHT ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAINFUL RESPIRATION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 1 FDA reports)
PANCREATIC CYST ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARALYSIS ( 1 FDA reports)
PARANASAL SINUS HYPERSECRETION ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PELVIC PAIN ( 1 FDA reports)
PENIS DISORDER ( 1 FDA reports)
POISONING ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYDIPSIA ( 1 FDA reports)
POLYMENORRHOEA ( 1 FDA reports)
POLYMYALGIA RHEUMATICA ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
PREMENSTRUAL SYNDROME ( 1 FDA reports)
PRESCRIBED OVERDOSE ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATE CANCER ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RED BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
RENAL FAILURE ( 1 FDA reports)
RESPIRATORY DEPRESSION ( 1 FDA reports)
RESPIRATORY TRACT INFECTION ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RIGHT VENTRICULAR FAILURE ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SENSITIVITY OF TEETH ( 1 FDA reports)
SHOULDER PAIN ( 1 FDA reports)
SICK SINUS SYNDROME ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN CANCER ( 1 FDA reports)
SKIN EXFOLIATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 1 FDA reports)
SOMNAMBULISM ( 1 FDA reports)
SPHINCTER OF ODDI DYSFUNCTION ( 1 FDA reports)
STEATORRHOEA ( 1 FDA reports)
STENT MALFUNCTION ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STRESS AT WORK ( 1 FDA reports)
STRESS SYMPTOMS ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SUTURE INSERTION ( 1 FDA reports)
SYNCOPE VASOVAGAL ( 1 FDA reports)
TACHYARRHYTHMIA ( 1 FDA reports)
TEMPOROMANDIBULAR JOINT SYNDROME ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
TENSION ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROMBOPHLEBITIS ( 1 FDA reports)
THYROIDECTOMY ( 1 FDA reports)
TONGUE DISORDER ( 1 FDA reports)
TONGUE EXFOLIATION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRIGGER FINGER ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETHRAL STENOSIS ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT NEOPLASM ( 1 FDA reports)
UTERINE SPASM ( 1 FDA reports)
VAGINAL BURNING SENSATION ( 1 FDA reports)
VAGINAL INFECTION ( 1 FDA reports)
VEIN DISORDER ( 1 FDA reports)
VENTRICULAR ASYSTOLE ( 1 FDA reports)
VIOLENCE-RELATED SYMPTOM ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISUAL BRIGHTNESS ( 1 FDA reports)
VITAMIN D ABNORMAL ( 1 FDA reports)
VITREOUS DETACHMENT ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
VOLVULUS ( 1 FDA reports)
VULVA CYST ( 1 FDA reports)
VULVOVAGINAL DISCOMFORT ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WEIGHT LOSS POOR ( 1 FDA reports)
WHITE BLOOD CELL COUNT ABNORMAL ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WRIST FRACTURE ( 1 FDA reports)
WRIST SURGERY ( 1 FDA reports)

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