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DRUG INEFFECTIVE ( 442 FDA reports)
DRUG EFFECT DECREASED ( 95 FDA reports)
INSOMNIA ( 94 FDA reports)
SOMNOLENCE ( 87 FDA reports)
OVERDOSE ( 77 FDA reports)
DIZZINESS ( 76 FDA reports)
FEELING ABNORMAL ( 73 FDA reports)
RESTLESSNESS ( 50 FDA reports)
MALAISE ( 40 FDA reports)
FATIGUE ( 37 FDA reports)
RESTLESS LEGS SYNDROME ( 37 FDA reports)
HEADACHE ( 32 FDA reports)
AGITATION ( 30 FDA reports)
CONDITION AGGRAVATED ( 30 FDA reports)
NAUSEA ( 29 FDA reports)
FEELING JITTERY ( 28 FDA reports)
ABDOMINAL PAIN UPPER ( 26 FDA reports)
PALPITATIONS ( 25 FDA reports)
ANXIETY ( 24 FDA reports)
HANGOVER ( 24 FDA reports)
NERVOUSNESS ( 24 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 22 FDA reports)
SWELLING FACE ( 22 FDA reports)
TREMOR ( 22 FDA reports)
VOMITING ( 22 FDA reports)
DRY MOUTH ( 19 FDA reports)
DYSPNOEA ( 19 FDA reports)
RASH ( 19 FDA reports)
URTICARIA ( 19 FDA reports)
DRUG EFFECT PROLONGED ( 18 FDA reports)
HYPOAESTHESIA ( 17 FDA reports)
PAIN ( 17 FDA reports)
PRURITUS ( 17 FDA reports)
BLISTER ( 16 FDA reports)
ERYTHEMA ( 16 FDA reports)
INCORRECT DOSE ADMINISTERED ( 16 FDA reports)
NIGHTMARE ( 15 FDA reports)
PAIN IN EXTREMITY ( 15 FDA reports)
BLOOD PRESSURE INCREASED ( 14 FDA reports)
HEART RATE INCREASED ( 14 FDA reports)
HYPERHIDROSIS ( 14 FDA reports)
HYPERSENSITIVITY ( 14 FDA reports)
ABDOMINAL DISCOMFORT ( 13 FDA reports)
DIARRHOEA ( 13 FDA reports)
DRUG DEPENDENCE ( 13 FDA reports)
ABNORMAL DREAMS ( 12 FDA reports)
BACK PAIN ( 12 FDA reports)
CHEST PAIN ( 12 FDA reports)
POOR QUALITY SLEEP ( 12 FDA reports)
PRODUCT QUALITY ISSUE ( 12 FDA reports)
DEPRESSION ( 11 FDA reports)
DISCOMFORT ( 11 FDA reports)
INTENTIONAL OVERDOSE ( 11 FDA reports)
BALANCE DISORDER ( 10 FDA reports)
CONVULSION ( 10 FDA reports)
DISORIENTATION ( 10 FDA reports)
DRUG SCREEN FALSE POSITIVE ( 10 FDA reports)
DYSPHAGIA ( 10 FDA reports)
FAECES DISCOLOURED ( 10 FDA reports)
FOREIGN BODY ( 10 FDA reports)
MIDDLE INSOMNIA ( 10 FDA reports)
MUSCLE SPASMS ( 10 FDA reports)
MYALGIA ( 10 FDA reports)
TINNITUS ( 10 FDA reports)
ACUTE CORONARY SYNDROME ( 9 FDA reports)
CONSTIPATION ( 9 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
DRUG INTOLERANCE ( 9 FDA reports)
EYE DISORDER ( 9 FDA reports)
EYE SWELLING ( 9 FDA reports)
IRRITABILITY ( 9 FDA reports)
PARANOIA ( 9 FDA reports)
PRURITUS GENERALISED ( 9 FDA reports)
PULMONARY HYPERTENSION ( 9 FDA reports)
WRONG DRUG ADMINISTERED ( 9 FDA reports)
ARTERIOSCLEROSIS CORONARY ARTERY ( 8 FDA reports)
ASTHENIA ( 8 FDA reports)
BURNING SENSATION ( 8 FDA reports)
CHOLECYSTITIS ( 8 FDA reports)
CORONARY ARTERY DISEASE ( 8 FDA reports)
DIASTOLIC DYSFUNCTION ( 8 FDA reports)
DYSPEPSIA ( 8 FDA reports)
FALL ( 8 FDA reports)
HAEMATOCHEZIA ( 8 FDA reports)
HALLUCINATION ( 8 FDA reports)
MEMORY IMPAIRMENT ( 8 FDA reports)
MUSCLE DISORDER ( 8 FDA reports)
MYOCARDIAL INFARCTION ( 8 FDA reports)
PULMONARY EMBOLISM ( 8 FDA reports)
THROAT IRRITATION ( 8 FDA reports)
TROPONIN INCREASED ( 8 FDA reports)
UNEVALUABLE EVENT ( 8 FDA reports)
VASCULITIS ( 8 FDA reports)
VISION BLURRED ( 8 FDA reports)
BLOOD GLUCOSE INCREASED ( 7 FDA reports)
CHOKING ( 7 FDA reports)
DYSURIA ( 7 FDA reports)
FLUSHING ( 7 FDA reports)
FORMICATION ( 7 FDA reports)
GASTRIC HAEMORRHAGE ( 7 FDA reports)
GLOSSODYNIA ( 7 FDA reports)
INAPPROPRIATE SCHEDULE OF DRUG ADMINISTRATION ( 7 FDA reports)
OEDEMA PERIPHERAL ( 7 FDA reports)
PARAESTHESIA ( 7 FDA reports)
PSYCHOTIC DISORDER ( 7 FDA reports)
ABDOMINAL PAIN ( 6 FDA reports)
ACCIDENTAL OVERDOSE ( 6 FDA reports)
AMNESIA ( 6 FDA reports)
ARTHRALGIA ( 6 FDA reports)
COELIAC DISEASE ( 6 FDA reports)
COUGH ( 6 FDA reports)
DIABETES MELLITUS ( 6 FDA reports)
DRUG ADMINISTRATION ERROR ( 6 FDA reports)
ENERGY INCREASED ( 6 FDA reports)
EXPIRED DRUG ADMINISTERED ( 6 FDA reports)
HAEMATEMESIS ( 6 FDA reports)
HYPERTENSION ( 6 FDA reports)
INFLUENZA ( 6 FDA reports)
INFLUENZA LIKE ILLNESS ( 6 FDA reports)
LETHARGY ( 6 FDA reports)
LIP SWELLING ( 6 FDA reports)
MUSCLE TWITCHING ( 6 FDA reports)
OROPHARYNGEAL PAIN ( 6 FDA reports)
VERTIGO ( 6 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 5 FDA reports)
CHEST DISCOMFORT ( 5 FDA reports)
DEHYDRATION ( 5 FDA reports)
FEELING HOT ( 5 FDA reports)
GAIT DISTURBANCE ( 5 FDA reports)
GASTRITIS ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
HYPERSOMNIA ( 5 FDA reports)
MENSTRUATION IRREGULAR ( 5 FDA reports)
MIGRAINE ( 5 FDA reports)
NASOPHARYNGITIS ( 5 FDA reports)
NIGHT SWEATS ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
SINUS HEADACHE ( 5 FDA reports)
SUICIDE ATTEMPT ( 5 FDA reports)
SWOLLEN TONGUE ( 5 FDA reports)
TACHYPHRENIA ( 5 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 5 FDA reports)
URINARY TRACT INFECTION ( 5 FDA reports)
ACCIDENTAL EXPOSURE ( 4 FDA reports)
ASTHENOPIA ( 4 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 4 FDA reports)
DEEP VEIN THROMBOSIS ( 4 FDA reports)
DEPENDENCE ( 4 FDA reports)
DRUG HYPERSENSITIVITY ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
FEAR ( 4 FDA reports)
FEELING COLD ( 4 FDA reports)
FEELING OF BODY TEMPERATURE CHANGE ( 4 FDA reports)
INJECTION SITE MASS ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
MUSCULAR WEAKNESS ( 4 FDA reports)
NASAL CONGESTION ( 4 FDA reports)
ORAL DISCOMFORT ( 4 FDA reports)
PHOTOPHOBIA ( 4 FDA reports)
PRODUCT LABEL ISSUE ( 4 FDA reports)
RASH ERYTHEMATOUS ( 4 FDA reports)
RETCHING ( 4 FDA reports)
WEIGHT INCREASED ( 4 FDA reports)
WHEEZING ( 4 FDA reports)
AGGRESSION ( 3 FDA reports)
ANKLE FRACTURE ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD SODIUM DECREASED ( 3 FDA reports)
CHILLS ( 3 FDA reports)
CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR ( 3 FDA reports)
CYSTITIS ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG ABUSE ( 3 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 3 FDA reports)
DYSGEUSIA ( 3 FDA reports)
EAR DISORDER ( 3 FDA reports)
ESCHERICHIA SEPSIS ( 3 FDA reports)
EUPHORIC MOOD ( 3 FDA reports)
EYE PRURITUS ( 3 FDA reports)
FALSE POSITIVE INVESTIGATION RESULT ( 3 FDA reports)
FEELING DRUNK ( 3 FDA reports)
FEELING OF RELAXATION ( 3 FDA reports)
GASTROINTESTINAL MOTILITY DISORDER ( 3 FDA reports)
GINGIVAL PAIN ( 3 FDA reports)
HAEMOPTYSIS ( 3 FDA reports)
HEAD INJURY ( 3 FDA reports)
HEART RATE IRREGULAR ( 3 FDA reports)
HYPERCHLORHYDRIA ( 3 FDA reports)
HYPERVIGILANCE ( 3 FDA reports)
INJECTION SITE ERYTHEMA ( 3 FDA reports)
INJECTION SITE SWELLING ( 3 FDA reports)
LIP BLISTER ( 3 FDA reports)
NO ADVERSE EVENT ( 3 FDA reports)
NON-CARDIAC CHEST PAIN ( 3 FDA reports)
NONSPECIFIC REACTION ( 3 FDA reports)
ORAL PAIN ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
PULMONARY INFARCTION ( 3 FDA reports)
RASH MACULAR ( 3 FDA reports)
RASH PRURITIC ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
RENAL PAIN ( 3 FDA reports)
ROAD TRAFFIC ACCIDENT ( 3 FDA reports)
SENSATION OF HEAVINESS ( 3 FDA reports)
STRESS ( 3 FDA reports)
TENSION ( 3 FDA reports)
TOOTHACHE ( 3 FDA reports)
VISUAL IMPAIRMENT ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
ABASIA ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
AMPHETAMINES POSITIVE ( 2 FDA reports)
ANAPHYLACTIC SHOCK ( 2 FDA reports)
APHAGIA ( 2 FDA reports)
APTYALISM ( 2 FDA reports)
AURICULAR SWELLING ( 2 FDA reports)
BLEPHAROSPASM ( 2 FDA reports)
BODY HEIGHT DECREASED ( 2 FDA reports)
CATARACT ( 2 FDA reports)
CEREBROVASCULAR ACCIDENT ( 2 FDA reports)
CHOLELITHIASIS ( 2 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 2 FDA reports)
COGNITIVE DISORDER ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
DEAFNESS ( 2 FDA reports)
DEATH ( 2 FDA reports)
DELUSION ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DEPRESSED MOOD ( 2 FDA reports)
DRUG ABUSER ( 2 FDA reports)
DRUG LABEL CONFUSION ( 2 FDA reports)
DRY SKIN ( 2 FDA reports)
DYSAESTHESIA ( 2 FDA reports)
DYSPNOEA EXERTIONAL ( 2 FDA reports)
EMOTIONAL DISTRESS ( 2 FDA reports)
EPISTAXIS ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 2 FDA reports)
GINGIVAL ERYTHEMA ( 2 FDA reports)
GINGIVAL SWELLING ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HERPES ZOSTER DISSEMINATED ( 2 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 2 FDA reports)
INFECTION ( 2 FDA reports)
INJECTION SITE PAIN ( 2 FDA reports)
INJURY ( 2 FDA reports)
INTENTIONAL DRUG MISUSE ( 2 FDA reports)
INTESTINAL OBSTRUCTION ( 2 FDA reports)
LIMB DISCOMFORT ( 2 FDA reports)
LISTLESS ( 2 FDA reports)
MARITAL PROBLEM ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MUSCLE SPASTICITY ( 2 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 2 FDA reports)
MYOCLONUS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NEUTROPENIA ( 2 FDA reports)
OCULAR HYPERAEMIA ( 2 FDA reports)
OEDEMA MOUTH ( 2 FDA reports)
OROPHARYNGEAL BLISTERING ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PARAPARESIS ( 2 FDA reports)
PERIPHERAL COLDNESS ( 2 FDA reports)
PERONEAL NERVE PALSY ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
PHOTOSENSITIVITY REACTION ( 2 FDA reports)
PHYSICAL PRODUCT LABEL ISSUE ( 2 FDA reports)
PNEUMONIA ( 2 FDA reports)
PRODUCT CLOSURE ISSUE ( 2 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 2 FDA reports)
PROSTATITIS ( 2 FDA reports)
PROSTATOMEGALY ( 2 FDA reports)
PURULENT DISCHARGE ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RENAL IMPAIRMENT ( 2 FDA reports)
SCREAMING ( 2 FDA reports)
SEDATION ( 2 FDA reports)
SENSORY DISTURBANCE ( 2 FDA reports)
SHOCK ( 2 FDA reports)
SLEEP DISORDER ( 2 FDA reports)
SLEEP TALKING ( 2 FDA reports)
SLUGGISHNESS ( 2 FDA reports)
SOMNAMBULISM ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STOMATITIS ( 2 FDA reports)
TESTICULAR PAIN ( 2 FDA reports)
THIRST ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOTAL LUNG CAPACITY DECREASED ( 2 FDA reports)
URINARY RETENTION ( 2 FDA reports)
VAGINAL HAEMORRHAGE ( 2 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 2 FDA reports)
ABNORMAL SLEEP-RELATED EVENT ( 1 FDA reports)
ABORTION SPONTANEOUS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
ALCOHOL INTOLERANCE ( 1 FDA reports)
ANAEMIA ( 1 FDA reports)
ANGINA PECTORIS ( 1 FDA reports)
ANGIOEDEMA ( 1 FDA reports)
ANORECTAL DISCOMFORT ( 1 FDA reports)
APATHY ( 1 FDA reports)
APHTHOUS STOMATITIS ( 1 FDA reports)
BASAL CELL CARCINOMA ( 1 FDA reports)
BILIARY COLIC ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD CALCIUM DECREASED ( 1 FDA reports)
BLOOD CREATINE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM ABNORMAL ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 1 FDA reports)
BLOOD TEST ABNORMAL ( 1 FDA reports)
BONE PAIN ( 1 FDA reports)
BREAST DISCHARGE ( 1 FDA reports)
BREATH ODOUR ( 1 FDA reports)
CAPSULE ISSUE ( 1 FDA reports)
CAROTID ARTERY OCCLUSION ( 1 FDA reports)
CELLULITIS ( 1 FDA reports)
CHOLECYSTITIS CHRONIC ( 1 FDA reports)
CLAUSTROPHOBIA ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
DECREASED APPETITE ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE ( 1 FDA reports)
DRUG DELIVERY SYSTEM MALFUNCTION ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL INCREASED ( 1 FDA reports)
DYSKINESIA ( 1 FDA reports)
DYSSTASIA ( 1 FDA reports)
EJACULATION DISORDER ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ENEMA ADMINISTRATION ( 1 FDA reports)
ERUCTATION ( 1 FDA reports)
EYE HAEMORRHAGE ( 1 FDA reports)
EYE MOVEMENT DISORDER ( 1 FDA reports)
EYELID SENSORY DISORDER ( 1 FDA reports)
FAECAL INCONTINENCE ( 1 FDA reports)
FAECALOMA ( 1 FDA reports)
FEAR OF DISEASE ( 1 FDA reports)
FLANK PAIN ( 1 FDA reports)
FLUID RETENTION ( 1 FDA reports)
FULL BLOOD COUNT DECREASED ( 1 FDA reports)
GASTRIC DISORDER ( 1 FDA reports)
GENERALISED ERYTHEMA ( 1 FDA reports)
GINGIVAL BLEEDING ( 1 FDA reports)
GLOBAL AMNESIA ( 1 FDA reports)
GLUCOSE TOLERANCE IMPAIRED ( 1 FDA reports)
HAEMORRHAGE ( 1 FDA reports)
HAEMORRHAGIC ANAEMIA ( 1 FDA reports)
HAEMORRHOIDS ( 1 FDA reports)
HEART RATE ABNORMAL ( 1 FDA reports)
HEPATIC ENZYME INCREASED ( 1 FDA reports)
HERPES ZOSTER ( 1 FDA reports)
HYPOTENSION ( 1 FDA reports)
IMMOBILE ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE HAEMATOMA ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INDURATION ( 1 FDA reports)
INJECTION SITE INFECTION ( 1 FDA reports)
INJECTION SITE REACTION ( 1 FDA reports)
INTERVERTEBRAL DISC DEGENERATION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY INFECTION ( 1 FDA reports)
LABYRINTHITIS ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGITIS ( 1 FDA reports)
LEUKOCYTOSIS ( 1 FDA reports)
LIPIDS INCREASED ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LUDWIG ANGINA ( 1 FDA reports)
LYMPHOCYTOSIS ( 1 FDA reports)
LYMPHOPLASMACYTOID LYMPHOMA/IMMUNOCYTOMA ( 1 FDA reports)
MALIGNANT MELANOMA ( 1 FDA reports)
MENSTRUATION DELAYED ( 1 FDA reports)
METABOLIC DISORDER ( 1 FDA reports)
MOOD ALTERED ( 1 FDA reports)
MOUTH HAEMORRHAGE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUCOSAL INFLAMMATION ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE RIGIDITY ( 1 FDA reports)
MUSCLE TIGHTNESS ( 1 FDA reports)
MUSCULOSKELETAL DISCOMFORT ( 1 FDA reports)
MUSCULOSKELETAL PAIN ( 1 FDA reports)
NASAL DRYNESS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NON-HODGKIN'S LYMPHOMA ( 1 FDA reports)
OEDEMA ( 1 FDA reports)
OESOPHAGEAL DISORDER ( 1 FDA reports)
OESOPHAGEAL PAIN ( 1 FDA reports)
OESOPHAGITIS ( 1 FDA reports)
OFF LABEL USE ( 1 FDA reports)
OPIATES POSITIVE ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
PALLOR ( 1 FDA reports)
PANIC REACTION ( 1 FDA reports)
PARAESTHESIA ORAL ( 1 FDA reports)
PARKINSON'S DISEASE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 1 FDA reports)
PHYSICAL ASSAULT ( 1 FDA reports)
PLATELET COUNT DECREASED ( 1 FDA reports)
POOR QUALITY DRUG ADMINISTERED ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PROCTALGIA ( 1 FDA reports)
PRODUCT COATING ISSUE ( 1 FDA reports)
PRODUCT LABEL ON WRONG PRODUCT ( 1 FDA reports)
PRODUCT SHAPE ISSUE ( 1 FDA reports)
PRODUCT TAMPERING ( 1 FDA reports)
PROSTATIC DISORDER ( 1 FDA reports)
PULMONARY FUNCTION TEST DECREASED ( 1 FDA reports)
RAPID EYE MOVEMENTS SLEEP ABNORMAL ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RECTAL HAEMORRHAGE ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SCAB ( 1 FDA reports)
SCROTAL SWELLING ( 1 FDA reports)
SEASONAL ALLERGY ( 1 FDA reports)
SKIN BURNING SENSATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SUNBURN ( 1 FDA reports)
SWELLING ( 1 FDA reports)
SYNCOPE ( 1 FDA reports)
TACHYCARDIA ( 1 FDA reports)
TEMPERATURE INTOLERANCE ( 1 FDA reports)
TENDERNESS ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE DRY ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRISMUS ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINE ODOUR ABNORMAL ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
WEIGHT DECREASED ( 1 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 1 FDA reports)

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