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

DIARRHOEA ( 37 FDA reports)
VOMITING ( 16 FDA reports)
DYSPNOEA ( 15 FDA reports)
HEADACHE ( 15 FDA reports)
ABDOMINAL PAIN UPPER ( 14 FDA reports)
NAUSEA ( 14 FDA reports)
PAIN ( 14 FDA reports)
PRURITUS ( 12 FDA reports)
DIZZINESS ( 10 FDA reports)
FATIGUE ( 10 FDA reports)
RASH ( 10 FDA reports)
DRUG INEFFECTIVE ( 9 FDA reports)
INSOMNIA ( 9 FDA reports)
DEEP VEIN THROMBOSIS ( 8 FDA reports)
SINUSITIS ( 8 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 7 FDA reports)
DYSPEPSIA ( 7 FDA reports)
HYPOTHYROIDISM ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PULMONARY EMBOLISM ( 7 FDA reports)
SEPSIS ( 7 FDA reports)
TYPE 2 DIABETES MELLITUS ( 7 FDA reports)
WEIGHT DECREASED ( 7 FDA reports)
ANAEMIA ( 6 FDA reports)
CARDIO-RESPIRATORY ARREST ( 6 FDA reports)
DYSPHAGIA ( 6 FDA reports)
ECONOMIC PROBLEM ( 6 FDA reports)
ERYTHEMA ( 6 FDA reports)
EYE INFECTION ( 6 FDA reports)
HYPERTHYROIDISM ( 6 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 6 FDA reports)
MEDICATION ERROR ( 6 FDA reports)
PARAESTHESIA ( 6 FDA reports)
PNEUMONIA ( 6 FDA reports)
VENTRICULAR FIBRILLATION ( 6 FDA reports)
ASTHENIA ( 5 FDA reports)
DRUG INTERACTION ( 5 FDA reports)
EAR PAIN ( 5 FDA reports)
MALAISE ( 5 FDA reports)
MENTAL STATUS CHANGES ( 5 FDA reports)
MUSCLE SPASMS ( 5 FDA reports)
PYREXIA ( 5 FDA reports)
RENAL FAILURE ( 5 FDA reports)
TREMOR ( 5 FDA reports)
UNRESPONSIVE TO STIMULI ( 5 FDA reports)
URTICARIA ( 5 FDA reports)
ABDOMINAL DISCOMFORT ( 4 FDA reports)
ANXIETY ( 4 FDA reports)
BACK PAIN ( 4 FDA reports)
BLOOD POTASSIUM DECREASED ( 4 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 4 FDA reports)
COUGH ( 4 FDA reports)
DEHYDRATION ( 4 FDA reports)
DIABETIC NEUROPATHY ( 4 FDA reports)
DISCOMFORT ( 4 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HERPES ZOSTER ( 4 FDA reports)
HYPOAESTHESIA ( 4 FDA reports)
JAUNDICE ( 4 FDA reports)
LETHARGY ( 4 FDA reports)
MULTIPLE INJURIES ( 4 FDA reports)
PROSTATOMEGALY ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
STRESS ( 4 FDA reports)
THROMBOCYTOPENIA ( 4 FDA reports)
URINARY TRACT INFECTION ( 4 FDA reports)
VERTIGO ( 4 FDA reports)
ARTHRALGIA ( 3 FDA reports)
BILIARY DYSKINESIA ( 3 FDA reports)
BIPOLAR DISORDER ( 3 FDA reports)
BLOOD BILIRUBIN INCREASED ( 3 FDA reports)
BLOOD GLUCOSE INCREASED ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CEREBROVASCULAR ACCIDENT ( 3 FDA reports)
CHEST PAIN ( 3 FDA reports)
CHROMATURIA ( 3 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 3 FDA reports)
COLLAPSE OF LUNG ( 3 FDA reports)
CONDITION AGGRAVATED ( 3 FDA reports)
CONSTIPATION ( 3 FDA reports)
CYANOSIS ( 3 FDA reports)
DEMENTIA ( 3 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 3 FDA reports)
DIABETIC RETINOPATHY ( 3 FDA reports)
DISABILITY ( 3 FDA reports)
DISORIENTATION ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
EAR INFECTION ( 3 FDA reports)
ELECTROLYTE IMBALANCE ( 3 FDA reports)
ERUCTATION ( 3 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 3 FDA reports)
GAIT DISTURBANCE ( 3 FDA reports)
GASTROINTESTINAL DISORDER ( 3 FDA reports)
GUILLAIN-BARRE SYNDROME ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HYPERSENSITIVITY ( 3 FDA reports)
IMPAIRED DRIVING ABILITY ( 3 FDA reports)
INFLUENZA LIKE ILLNESS ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
LOSS OF CONSCIOUSNESS ( 3 FDA reports)
LUNG INFILTRATION ( 3 FDA reports)
LUNG NEOPLASM MALIGNANT ( 3 FDA reports)
NERVOUSNESS ( 3 FDA reports)
ORAL CANDIDIASIS ( 3 FDA reports)
OSTEOARTHRITIS ( 3 FDA reports)
PALPITATIONS ( 3 FDA reports)
PERIPHERAL COLDNESS ( 3 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 3 FDA reports)
POST PROCEDURAL COMPLICATION ( 3 FDA reports)
RESPIRATORY FAILURE ( 3 FDA reports)
SINUS TACHYCARDIA ( 3 FDA reports)
SURGERY ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TOOTH DISCOLOURATION ( 3 FDA reports)
TRANSPOSITION OF THE GREAT VESSELS ( 3 FDA reports)
TYPE 1 DIABETES MELLITUS ( 3 FDA reports)
WEIGHT INCREASED ( 3 FDA reports)
ABDOMINAL DISTENSION ( 2 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABDOMINAL TENDERNESS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ADVERSE EVENT ( 2 FDA reports)
AGITATION ( 2 FDA reports)
AMNESIA ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
APHASIA ( 2 FDA reports)
ARTERIOSCLEROSIS ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ATRIAL FIBRILLATION ( 2 FDA reports)
BLOOD PRESSURE DECREASED ( 2 FDA reports)
BRAIN NATRIURETIC PEPTIDE INCREASED ( 2 FDA reports)
BREATH SOUNDS ABNORMAL ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CANDIDIASIS ( 2 FDA reports)
CARDIAC MURMUR ( 2 FDA reports)
CELLULITIS ( 2 FDA reports)
CHEST DISCOMFORT ( 2 FDA reports)
CHOLANGITIS ( 2 FDA reports)
CHOLECYSTITIS CHRONIC ( 2 FDA reports)
CHOLESTASIS ( 2 FDA reports)
CONFUSIONAL STATE ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DEPRESSION ( 2 FDA reports)
DRUG HYPERSENSITIVITY ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
FACIAL PAIN ( 2 FDA reports)
FALL ( 2 FDA reports)
FEELING ABNORMAL ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FUNGAL INFECTION ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GALLBLADDER INJURY ( 2 FDA reports)
GANGRENE ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GROWTH RETARDATION ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HEPATIC STEATOSIS ( 2 FDA reports)
HUNGER ( 2 FDA reports)
IMPAIRED WORK ABILITY ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INFLAMMATION ( 2 FDA reports)
INJURY ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LIVEDO RETICULARIS ( 2 FDA reports)
MUSCULAR WEAKNESS ( 2 FDA reports)
MUSCULOSKELETAL PAIN ( 2 FDA reports)
NIGHT SWEATS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PARALYSIS ( 2 FDA reports)
PHARYNGEAL ERYTHEMA ( 2 FDA reports)
POSTNASAL DRIP ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PUPIL FIXED ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH GENERALISED ( 2 FDA reports)
RECTAL HAEMORRHAGE ( 2 FDA reports)
RETCHING ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
SKIN WARM ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SYNCOPE ( 2 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 2 FDA reports)
THYROIDITIS SUBACUTE ( 2 FDA reports)
TONGUE DISCOLOURATION ( 2 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 2 FDA reports)
WHEEZING ( 2 FDA reports)
WOUND DRAINAGE ( 2 FDA reports)
ABDOMINAL WALL HAEMATOMA ( 1 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABSCESS LIMB ( 1 FDA reports)
ACHOLIA ( 1 FDA reports)
ACUTE FEBRILE NEUTROPHILIC DERMATOSIS ( 1 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ALCOHOL USE ( 1 FDA reports)
ALOPECIA ( 1 FDA reports)
ANAEMIA POSTOPERATIVE ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL FISSURE ( 1 FDA reports)
ANAPHYLACTIC REACTION ( 1 FDA reports)
ANKYLOSING SPONDYLITIS ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATELECTASIS ( 1 FDA reports)
ATRIAL SEPTAL DEFECT ( 1 FDA reports)
BACK INJURY ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BENIGN PROSTATIC HYPERPLASIA ( 1 FDA reports)
BILIRUBIN CONJUGATED INCREASED ( 1 FDA reports)
BLADDER CANCER ( 1 FDA reports)
BLADDER MASS ( 1 FDA reports)
BLADDER NEOPLASM ( 1 FDA reports)
BLISTER ( 1 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 1 FDA reports)
BLOOD CULTURE POSITIVE ( 1 FDA reports)
BLOOD MAGNESIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE INCREASED ( 1 FDA reports)
BLOOD URINE PRESENT ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BRADYARRHYTHMIA ( 1 FDA reports)
BRADYCARDIA ( 1 FDA reports)
BRONCHOSPASM ( 1 FDA reports)
CARDIAC ARREST ( 1 FDA reports)
CARDIAC DISORDER ( 1 FDA reports)
CARDIAC PACEMAKER INSERTION ( 1 FDA reports)
CARDIAC VALVE DISEASE ( 1 FDA reports)
CARDIOMEGALY ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CAROTID ENDARTERECTOMY ( 1 FDA reports)
CARPAL TUNNEL SYNDROME ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTITIS ( 1 FDA reports)
CHOLELITHIASIS ( 1 FDA reports)
CHRONIC HEPATITIS ( 1 FDA reports)
CLOSTRIDIAL INFECTION ( 1 FDA reports)
COLONIC POLYP ( 1 FDA reports)
COMPUTERISED TOMOGRAM ABNORMAL ( 1 FDA reports)
CONGENITAL CENTRAL NERVOUS SYSTEM ANOMALY ( 1 FDA reports)
CONTUSION ( 1 FDA reports)
CONVERSION DISORDER ( 1 FDA reports)
CORONARY ARTERY DISEASE ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CUBITAL TUNNEL SYNDROME ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 1 FDA reports)
DIABETES MELLITUS ( 1 FDA reports)
DIABETIC COMPLICATION ( 1 FDA reports)
DIABETIC FOOT INFECTION ( 1 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 1 FDA reports)
DILATATION ATRIAL ( 1 FDA reports)
DILATATION VENTRICULAR ( 1 FDA reports)
DISEASE COMPLICATION ( 1 FDA reports)
DISTURBANCE IN ATTENTION ( 1 FDA reports)
DIVERTICULITIS ( 1 FDA reports)
DIVERTICULUM ( 1 FDA reports)
DIVORCED ( 1 FDA reports)
DRUG ABUSE ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EFFECT DECREASED ( 1 FDA reports)
DRUG EXPOSURE VIA BREAST MILK ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRUG TOXICITY ( 1 FDA reports)
DRY MOUTH ( 1 FDA reports)
DYSGEUSIA ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSPNOEA EXERTIONAL ( 1 FDA reports)
EAR DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM Q WAVES ( 1 FDA reports)
ENDARTERECTOMY ( 1 FDA reports)
ENTEROCOLITIS HAEMORRHAGIC ( 1 FDA reports)
ERYTHEMA OF EYELID ( 1 FDA reports)
EXCORIATION ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXOSTOSIS ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEMORAL ARTERIAL STENOSIS ( 1 FDA reports)
FEMORAL ARTERY OCCLUSION ( 1 FDA reports)
FLUSHING ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GASTROENTERITIS VIRAL ( 1 FDA reports)
GENITAL PRURITUS FEMALE ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMATOCRIT DECREASED ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAEMORRHOIDAL HAEMORRHAGE ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HALLUCINATION ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEART RATE IRREGULAR ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATITIS ( 1 FDA reports)
HEPATITIS ACUTE ( 1 FDA reports)
HEPATITIS B ( 1 FDA reports)
HEPATITIS VIRAL ( 1 FDA reports)
HEPATOTOXICITY ( 1 FDA reports)
HICCUPS ( 1 FDA reports)
HIV INFECTION ( 1 FDA reports)
HODGKIN'S DISEASE ( 1 FDA reports)
HYPERAESTHESIA ( 1 FDA reports)
HYPERGLYCAEMIA ( 1 FDA reports)
HYPERHIDROSIS ( 1 FDA reports)
HYPERNATRAEMIA ( 1 FDA reports)
HYPERPLASIA ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPERTENSION ( 1 FDA reports)
HYPOACUSIS ( 1 FDA reports)
HYPOAESTHESIA ORAL ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOKALAEMIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
HYPOXIA ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNE SYSTEM DISORDER ( 1 FDA reports)
INCORRECT DOSE ADMINISTERED ( 1 FDA reports)
INFLUENZA ( 1 FDA reports)
INJECTION SITE PRURITUS ( 1 FDA reports)
INSULIN RESISTANCE ( 1 FDA reports)
INTERCEPTED MEDICATION ERROR ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTERSTITIAL LUNG DISEASE ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
ISCHAEMIA ( 1 FDA reports)
ISCHAEMIC CARDIOMYOPATHY ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT DISLOCATION ( 1 FDA reports)
JOINT RANGE OF MOTION DECREASED ( 1 FDA reports)
JUDGEMENT IMPAIRED ( 1 FDA reports)
KIDNEY FIBROSIS ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ABNORMAL ( 1 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEG AMPUTATION ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIVER INJURY ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUNG ADENOCARCINOMA ( 1 FDA reports)
LYME DISEASE ( 1 FDA reports)
MALIGNANT NEOPLASM PROGRESSION ( 1 FDA reports)
MARITAL PROBLEM ( 1 FDA reports)
MEDICATION RESIDUE ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MICTURITION URGENCY ( 1 FDA reports)
MIDDLE INSOMNIA ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MONOPARESIS ( 1 FDA reports)
MOOD SWINGS ( 1 FDA reports)
MOUTH ULCERATION ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE ATROPHY ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYALGIA ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOCARDIAL INFARCTION ( 1 FDA reports)
MYOCARDIAL ISCHAEMIA ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NECK PAIN ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
NODAL RHYTHM ( 1 FDA reports)
NORMOCHROMIC NORMOCYTIC ANAEMIA ( 1 FDA reports)
OBESITY ( 1 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 1 FDA reports)
OBSTRUCTION ( 1 FDA reports)
OBSTRUCTIVE AIRWAYS DISORDER ( 1 FDA reports)
OLIGURIA ( 1 FDA reports)
ONCOLOGIC COMPLICATION ( 1 FDA reports)
OROPHARYNGEAL SWELLING ( 1 FDA reports)
ORTHOPNOEA ( 1 FDA reports)
ORTHOSTATIC INTOLERANCE ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPENIA ( 1 FDA reports)
OTITIS EXTERNA ( 1 FDA reports)
OTITIS MEDIA ACUTE ( 1 FDA reports)
OXYGEN SATURATION ABNORMAL ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANCREATIC ENLARGEMENT ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PICKWICKIAN SYNDROME ( 1 FDA reports)
PLEURAL EFFUSION ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POLYCYSTIC OVARIES ( 1 FDA reports)
POOR QUALITY SLEEP ( 1 FDA reports)
POST PROCEDURAL DISCOMFORT ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT ODOUR ABNORMAL ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC OBSTRUCTION ( 1 FDA reports)
PROTHROMBIN LEVEL INCREASED ( 1 FDA reports)
PROTHROMBIN TIME PROLONGED ( 1 FDA reports)
PRURITUS ANI ( 1 FDA reports)
PRURITUS GENERALISED ( 1 FDA reports)
PSEUDOMONAS INFECTION ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PULMONARY CONGESTION ( 1 FDA reports)
PULMONARY HYPERTENSION ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
PULMONARY VALVE STENOSIS ( 1 FDA reports)
PULSE ABSENT ( 1 FDA reports)
RALES ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY TRACT CONGESTION ( 1 FDA reports)
RESTLESS LEGS SYNDROME ( 1 FDA reports)
RHINITIS ( 1 FDA reports)
RHINITIS ALLERGIC ( 1 FDA reports)
RHONCHI ( 1 FDA reports)
RIB FRACTURE ( 1 FDA reports)
ROAD TRAFFIC ACCIDENT ( 1 FDA reports)
ROTATOR CUFF SYNDROME ( 1 FDA reports)
SCAN MYOCARDIAL PERFUSION ABNORMAL ( 1 FDA reports)
SENSATION OF FOREIGN BODY ( 1 FDA reports)
SEPTIC SHOCK ( 1 FDA reports)
SINUS ARRHYTHMIA ( 1 FDA reports)
SINUS BRADYCARDIA ( 1 FDA reports)
SINUS CONGESTION ( 1 FDA reports)
SINUS DISORDER ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SKIN LACERATION ( 1 FDA reports)
SKIN LESION ( 1 FDA reports)
SKIN ULCER ( 1 FDA reports)
SLEEP APNOEA SYNDROME ( 1 FDA reports)
SLEEP DISORDER ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
STATUS EPILEPTICUS ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
STEVENS-JOHNSON SYNDROME ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRIDOR ( 1 FDA reports)
SUICIDAL IDEATION ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
SWOLLEN TONGUE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TACHYPNOEA ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THERAPEUTIC RESPONSE DELAYED ( 1 FDA reports)
THIRST ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DESQUAMATION ( 1 FDA reports)
TOOTH ABSCESS ( 1 FDA reports)
TOXIC SKIN ERUPTION ( 1 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 1 FDA reports)
TRICUSPID VALVE INCOMPETENCE ( 1 FDA reports)
UNEVALUABLE EVENT ( 1 FDA reports)
UPPER AIRWAY RESISTANCE SYNDROME ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
UPPER-AIRWAY COUGH SYNDROME ( 1 FDA reports)
URTICARIA GENERALISED ( 1 FDA reports)
VAGINAL HAEMORRHAGE ( 1 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VENTRICULAR SEPTAL DEFECT ( 1 FDA reports)
VENTRICULAR TACHYCARDIA ( 1 FDA reports)
VIITH NERVE PARALYSIS ( 1 FDA reports)
VISION BLURRED ( 1 FDA reports)
VULVOVAGINAL MYCOTIC INFECTION ( 1 FDA reports)
WOUND ( 1 FDA reports)
WOUND INFECTION ( 1 FDA reports)
YELLOW SKIN ( 1 FDA reports)

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