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

DEPRESSION ( 22 FDA reports)
CONVULSION ( 19 FDA reports)
NAUSEA ( 18 FDA reports)
ANXIETY ( 16 FDA reports)
DRUG WITHDRAWAL SYNDROME NEONATAL ( 15 FDA reports)
GAIT DISTURBANCE ( 13 FDA reports)
HALLUCINATION ( 13 FDA reports)
SURGERY ( 13 FDA reports)
DIARRHOEA ( 12 FDA reports)
DRUG TOXICITY ( 12 FDA reports)
BLISTER ( 11 FDA reports)
CELLULITIS ( 11 FDA reports)
CEREBROVASCULAR ACCIDENT ( 11 FDA reports)
FALL ( 11 FDA reports)
LIMB INJURY ( 11 FDA reports)
BLUE TOE SYNDROME ( 10 FDA reports)
DRUG INEFFECTIVE ( 10 FDA reports)
DYSARTHRIA ( 10 FDA reports)
ELECTROLYTE IMBALANCE ( 10 FDA reports)
EMPHYSEMA ( 10 FDA reports)
HEADACHE ( 10 FDA reports)
LOCALISED INFECTION ( 10 FDA reports)
PANIC ATTACK ( 10 FDA reports)
DRUG INTERACTION ( 9 FDA reports)
POOR PERIPHERAL CIRCULATION ( 9 FDA reports)
PULSE ABSENT ( 9 FDA reports)
RENAL FAILURE ( 9 FDA reports)
THINKING ABNORMAL ( 9 FDA reports)
VISUAL ACUITY REDUCED ( 9 FDA reports)
BALANCE DISORDER ( 8 FDA reports)
DYSPNOEA ( 8 FDA reports)
MALAISE ( 8 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 7 FDA reports)
DIZZINESS ( 7 FDA reports)
VENOUS INSUFFICIENCY ( 7 FDA reports)
WEIGHT INCREASED ( 7 FDA reports)
BACK PAIN ( 6 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 6 FDA reports)
COMPLETED SUICIDE ( 6 FDA reports)
DEHYDRATION ( 6 FDA reports)
DISTURBANCE IN ATTENTION ( 6 FDA reports)
LOSS OF CONSCIOUSNESS ( 6 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 6 FDA reports)
RHABDOMYOLYSIS ( 6 FDA reports)
AGITATION ( 5 FDA reports)
APPLICATION SITE ERYTHEMA ( 5 FDA reports)
BLOOD CREATININE INCREASED ( 5 FDA reports)
DRUG DEPENDENCE ( 5 FDA reports)
FATIGUE ( 5 FDA reports)
FEELING ABNORMAL ( 5 FDA reports)
HIP FRACTURE ( 5 FDA reports)
INSOMNIA ( 5 FDA reports)
MYOCARDIAL INFARCTION ( 5 FDA reports)
PARAESTHESIA ( 5 FDA reports)
ABDOMINAL PAIN UPPER ( 4 FDA reports)
CHEST PAIN ( 4 FDA reports)
CHOLECYSTECTOMY ( 4 FDA reports)
COLITIS ( 4 FDA reports)
CONDITION AGGRAVATED ( 4 FDA reports)
CRYING ( 4 FDA reports)
DEATH ( 4 FDA reports)
DRUG SCREEN POSITIVE ( 4 FDA reports)
DRY EYE ( 4 FDA reports)
FACIAL PALSY ( 4 FDA reports)
GLOMERULAR FILTRATION RATE DECREASED ( 4 FDA reports)
HYPERSENSITIVITY ( 4 FDA reports)
HYPERTENSION ( 4 FDA reports)
INFECTION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MEMORY IMPAIRMENT ( 4 FDA reports)
PAIN ( 4 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 4 FDA reports)
PYREXIA ( 4 FDA reports)
SKIN EXFOLIATION ( 4 FDA reports)
SUICIDE ATTEMPT ( 4 FDA reports)
TREMOR ( 4 FDA reports)
UNEVALUABLE EVENT ( 4 FDA reports)
VOMITING ( 4 FDA reports)
ABASIA ( 3 FDA reports)
APPLICATION SITE SWELLING ( 3 FDA reports)
BLOOD GLUCOSE ABNORMAL ( 3 FDA reports)
BLOOD PRESSURE INCREASED ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC DISORDER ( 3 FDA reports)
COGNITIVE DISORDER ( 3 FDA reports)
COMPLICATION OF PREGNANCY ( 3 FDA reports)
DEAFNESS ( 3 FDA reports)
ERECTILE DYSFUNCTION ( 3 FDA reports)
HEPATIC FUNCTION ABNORMAL ( 3 FDA reports)
HYPOAESTHESIA ( 3 FDA reports)
ILL-DEFINED DISORDER ( 3 FDA reports)
INTENTIONAL DRUG MISUSE ( 3 FDA reports)
JAUNDICE ( 3 FDA reports)
LIVER DISORDER ( 3 FDA reports)
MUSCLE SPASMS ( 3 FDA reports)
OFF LABEL USE ( 3 FDA reports)
POISONING DELIBERATE ( 3 FDA reports)
RENAL DISORDER ( 3 FDA reports)
SALIVARY HYPERSECRETION ( 3 FDA reports)
SKIN BURNING SENSATION ( 3 FDA reports)
SOMNOLENCE ( 3 FDA reports)
SWELLING ( 3 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 3 FDA reports)
VENOUS STASIS ( 3 FDA reports)
VIITH NERVE PARALYSIS ( 3 FDA reports)
WITHDRAWAL SYNDROME ( 3 FDA reports)
WRONG TECHNIQUE IN DRUG USAGE PROCESS ( 3 FDA reports)
ABDOMINAL PAIN ( 2 FDA reports)
ABORTION SPONTANEOUS ( 2 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 2 FDA reports)
ACUTE HEPATIC FAILURE ( 2 FDA reports)
ACUTE RESPIRATORY DISTRESS SYNDROME ( 2 FDA reports)
AGEUSIA ( 2 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ALOPECIA ( 2 FDA reports)
ANGER ( 2 FDA reports)
ANGIOPATHY ( 2 FDA reports)
APPLICATION SITE BURN ( 2 FDA reports)
ARRHYTHMIA ( 2 FDA reports)
ARTHRITIS ( 2 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 2 FDA reports)
ASTHENIA ( 2 FDA reports)
ATTENTION DEFICIT/HYPERACTIVITY DISORDER ( 2 FDA reports)
BEREAVEMENT REACTION ( 2 FDA reports)
BONE DISORDER ( 2 FDA reports)
BONE GIANT CELL TUMOUR ( 2 FDA reports)
BRONCHITIS ( 2 FDA reports)
CAUSTIC INJURY ( 2 FDA reports)
CEREBELLAR INFARCTION ( 2 FDA reports)
CEREBRAL HAEMORRHAGE ( 2 FDA reports)
CEREBRAL INFARCTION ( 2 FDA reports)
CHEMOTHERAPY ( 2 FDA reports)
CHEST INJURY ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLD SWEAT ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COUGH ( 2 FDA reports)
DANDRUFF ( 2 FDA reports)
DEAFNESS NEUROSENSORY ( 2 FDA reports)
DIABETES MELLITUS ( 2 FDA reports)
DRUG ABUSE ( 2 FDA reports)
DRY MOUTH ( 2 FDA reports)
DYSGEUSIA ( 2 FDA reports)
ESSENTIAL HYPERTENSION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE PAIN ( 2 FDA reports)
FLATULENCE ( 2 FDA reports)
FOOD ALLERGY ( 2 FDA reports)
FOOD INTERACTION ( 2 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 2 FDA reports)
GASTROINTESTINAL NECROSIS ( 2 FDA reports)
GLOMERULAR FILTRATION RATE INCREASED ( 2 FDA reports)
GRAND MAL CONVULSION ( 2 FDA reports)
HEAD DISCOMFORT ( 2 FDA reports)
HEART RATE INCREASED ( 2 FDA reports)
HYPERAESTHESIA ( 2 FDA reports)
HYPERBILIRUBINAEMIA ( 2 FDA reports)
HYPERCHOLESTEROLAEMIA ( 2 FDA reports)
HYPERGLYCAEMIA ( 2 FDA reports)
HYPERHIDROSIS ( 2 FDA reports)
HYPOAESTHESIA ORAL ( 2 FDA reports)
INFLUENZA ( 2 FDA reports)
INTENTIONAL OVERDOSE ( 2 FDA reports)
INTESTINAL FUNCTIONAL DISORDER ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
LIP DISORDER ( 2 FDA reports)
LIP PAIN ( 2 FDA reports)
LIP SWELLING ( 2 FDA reports)
LUNG DISORDER ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
MILK-ALKALI SYNDROME ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MOUTH INJURY ( 2 FDA reports)
MUSCLE INJURY ( 2 FDA reports)
MYALGIA ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NERVE INJURY ( 2 FDA reports)
NIGHTMARE ( 2 FDA reports)
NON-SMALL CELL LUNG CANCER ( 2 FDA reports)
OEDEMA PERIPHERAL ( 2 FDA reports)
ORAL DISCOMFORT ( 2 FDA reports)
ORAL PAIN ( 2 FDA reports)
OSTEOARTHRITIS ( 2 FDA reports)
PAIN IN EXTREMITY ( 2 FDA reports)
PALLOR ( 2 FDA reports)
PERIPHERAL ARTERIAL OCCLUSIVE DISEASE ( 2 FDA reports)
PHARYNGEAL OEDEMA ( 2 FDA reports)
POISONING ( 2 FDA reports)
PRODUCT QUALITY ISSUE ( 2 FDA reports)
PROSTATE CANCER ( 2 FDA reports)
PRURITUS ( 2 FDA reports)
PRURITUS GENERALISED ( 2 FDA reports)
RASH ( 2 FDA reports)
RENAL INJURY ( 2 FDA reports)
RESPIRATORY ARREST ( 2 FDA reports)
STENT PLACEMENT ( 2 FDA reports)
STEVENS-JOHNSON SYNDROME ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
STRESS ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
TACHYCARDIA ( 2 FDA reports)
THERAPEUTIC RESPONSE UNEXPECTED ( 2 FDA reports)
TONGUE DISORDER ( 2 FDA reports)
TONGUE OEDEMA ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
VISION BLURRED ( 2 FDA reports)
WEIGHT DECREASED ( 2 FDA reports)
ABNORMAL BEHAVIOUR ( 1 FDA reports)
ABNORMAL DREAMS ( 1 FDA reports)
ACCIDENTAL DRUG INTAKE BY CHILD ( 1 FDA reports)
ADRENAL DISORDER ( 1 FDA reports)
ADRENAL INSUFFICIENCY ( 1 FDA reports)
ADVERSE EVENT ( 1 FDA reports)
AFFECT LABILITY ( 1 FDA reports)
AFFECTIVE DISORDER ( 1 FDA reports)
AGGRESSION ( 1 FDA reports)
ALCOHOL POISONING ( 1 FDA reports)
ALTERED STATE OF CONSCIOUSNESS ( 1 FDA reports)
AMENORRHOEA ( 1 FDA reports)
AMNESIA ( 1 FDA reports)
ANHEDONIA ( 1 FDA reports)
ANOREXIA ( 1 FDA reports)
ANTICONVULSANT DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
ANTISOCIAL BEHAVIOUR ( 1 FDA reports)
ANURIA ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPENDICECTOMY ( 1 FDA reports)
APPLICATION SITE IRRITATION ( 1 FDA reports)
APPLICATION SITE PAIN ( 1 FDA reports)
APPLICATION SITE RASH ( 1 FDA reports)
APPLICATION SITE VESICLES ( 1 FDA reports)
ARTERIOSCLEROSIS ( 1 FDA reports)
ASPIRATION ( 1 FDA reports)
ATAXIA ( 1 FDA reports)
ATRIAL FIBRILLATION ( 1 FDA reports)
AURICULAR SWELLING ( 1 FDA reports)
BALANOPOSTHITIS ( 1 FDA reports)
BARIUM SWALLOW ABNORMAL ( 1 FDA reports)
BIPOLAR DISORDER ( 1 FDA reports)
BLADDER IRRITATION ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLOOD ELECTROLYTES DECREASED ( 1 FDA reports)
BLOOD GLUCOSE FLUCTUATION ( 1 FDA reports)
BLOOD GLUCOSE INCREASED ( 1 FDA reports)
BLOOD LACTATE DEHYDROGENASE INCREASED ( 1 FDA reports)
BLOOD POTASSIUM INCREASED ( 1 FDA reports)
BLOOD TRIGLYCERIDES INCREASED ( 1 FDA reports)
BODY HEIGHT DECREASED ( 1 FDA reports)
BODY HEIGHT INCREASED ( 1 FDA reports)
BODY TEMPERATURE DECREASED ( 1 FDA reports)
BONE METABOLISM DISORDER ( 1 FDA reports)
BURNING SENSATION ( 1 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 1 FDA reports)
CALCINOSIS ( 1 FDA reports)
CANDIDIASIS ( 1 FDA reports)
CARDIO-RESPIRATORY ARREST ( 1 FDA reports)
CARDIOVASCULAR DISORDER ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHILLS ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
CLUMSINESS ( 1 FDA reports)
COELIAC DISEASE ( 1 FDA reports)
COLECTOMY ( 1 FDA reports)
CONFUSIONAL STATE ( 1 FDA reports)
CONSTIPATION ( 1 FDA reports)
COORDINATION ABNORMAL ( 1 FDA reports)
CYST ( 1 FDA reports)
DECREASED ACTIVITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DEPENDENCE ( 1 FDA reports)
DEPRESSED MOOD ( 1 FDA reports)
DERMAL CYST ( 1 FDA reports)
DERMATITIS ALLERGIC ( 1 FDA reports)
DEVICE RELATED INFECTION ( 1 FDA reports)
DIFFICULTY IN WALKING ( 1 FDA reports)
DISEASE PROGRESSION ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG EXPOSURE DURING PREGNANCY ( 1 FDA reports)
DRUG HYPERSENSITIVITY ( 1 FDA reports)
DRUG INEFFECTIVE FOR UNAPPROVED INDICATION ( 1 FDA reports)
DRUG LEVEL BELOW THERAPEUTIC ( 1 FDA reports)
DRUG LEVEL DECREASED ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DYSPEPSIA ( 1 FDA reports)
DYSURIA ( 1 FDA reports)
EAR HAEMORRHAGE ( 1 FDA reports)
EAR PAIN ( 1 FDA reports)
EMOTIONAL DISTRESS ( 1 FDA reports)
EOSINOPHILIA ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EYE SWELLING ( 1 FDA reports)
FACE INJURY ( 1 FDA reports)
FAILURE TO THRIVE ( 1 FDA reports)
FEMUR FRACTURE ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FORMICATION ( 1 FDA reports)
FRACTURE DISPLACEMENT ( 1 FDA reports)
GASTRECTOMY ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL INFECTION ( 1 FDA reports)
GASTROINTESTINAL ULCER HAEMORRHAGE ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GROWTH ACCELERATED ( 1 FDA reports)
GROWTH OF EYELASHES ( 1 FDA reports)
HAEMODIALYSIS ( 1 FDA reports)
HAEMOLYSIS ( 1 FDA reports)
HAEMOPTYSIS ( 1 FDA reports)
HAIR GROWTH ABNORMAL ( 1 FDA reports)
HAIR TEXTURE ABNORMAL ( 1 FDA reports)
HERNIA ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HOSTILITY ( 1 FDA reports)
HYPERSOMNIA ( 1 FDA reports)
HYPOALBUMINAEMIA ( 1 FDA reports)
HYPOGLYCAEMIA ( 1 FDA reports)
HYPOMANIA ( 1 FDA reports)
HYPOPHAGIA ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOVOLAEMIA ( 1 FDA reports)
IDIOSYNCRATIC DRUG REACTION ( 1 FDA reports)
ILLUSION ( 1 FDA reports)
IMPAIRED DRIVING ABILITY ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
IMPATIENCE ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 1 FDA reports)
INFLAMMATION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INITIAL INSOMNIA ( 1 FDA reports)
INJECTION SITE PAIN ( 1 FDA reports)
INNER EAR DISORDER ( 1 FDA reports)
INTENTIONAL MISUSE ( 1 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 1 FDA reports)
INTRAOCULAR PRESSURE INCREASED ( 1 FDA reports)
INTRAOCULAR PRESSURE TEST ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KNEE OPERATION ( 1 FDA reports)
LACRIMATION INCREASED ( 1 FDA reports)
LARYNGEAL ERYTHEMA ( 1 FDA reports)
LETHARGY ( 1 FDA reports)
LIBIDO DECREASED ( 1 FDA reports)
LOBAR PNEUMONIA ( 1 FDA reports)
LOCAL SWELLING ( 1 FDA reports)
LOW TURNOVER OSTEOPATHY ( 1 FDA reports)
MALE SEXUAL DYSFUNCTION ( 1 FDA reports)
MANIA ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MENTAL IMPAIRMENT ( 1 FDA reports)
MULTI-ORGAN DISORDER ( 1 FDA reports)
MULTIPLE DRUG OVERDOSE INTENTIONAL ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MUSCULAR WEAKNESS ( 1 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
NAIL GROWTH ABNORMAL ( 1 FDA reports)
NASOPHARYNGEAL DISORDER ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEOPLASM MALIGNANT ( 1 FDA reports)
NEOPLASM PROGRESSION ( 1 FDA reports)
NEPHROPATHY ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NERVOUSNESS ( 1 FDA reports)
NEUROPATHY PERIPHERAL ( 1 FDA reports)
NEUTROPENIA ( 1 FDA reports)
NOCTURIA ( 1 FDA reports)
ORAL DYSAESTHESIA ( 1 FDA reports)
ORAL INTAKE REDUCED ( 1 FDA reports)
ORAL MUCOSAL EXFOLIATION ( 1 FDA reports)
ORGASM ABNORMAL ( 1 FDA reports)
OSTEOMYELITIS ( 1 FDA reports)
OSTEOPOROSIS ( 1 FDA reports)
OXYGEN SATURATION DECREASED ( 1 FDA reports)
PAIN IN JAW ( 1 FDA reports)
PANCYTOPENIA ( 1 FDA reports)
PARANOIA ( 1 FDA reports)
PAROSMIA ( 1 FDA reports)
PARTIAL SEIZURES ( 1 FDA reports)
PATHOLOGICAL FRACTURE ( 1 FDA reports)
PERSONALITY CHANGE ( 1 FDA reports)
PERSONALITY DISORDER ( 1 FDA reports)
PHAGOPHOBIA ( 1 FDA reports)
PHARMACEUTICAL PRODUCT COUNTERFEIT ( 1 FDA reports)
PLANTAR FASCIITIS ( 1 FDA reports)
PNEUMONIA ( 1 FDA reports)
PO2 DECREASED ( 1 FDA reports)
POLLAKIURIA ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST PROCEDURAL INFECTION ( 1 FDA reports)
PRESYNCOPE ( 1 FDA reports)
PROSTRATION ( 1 FDA reports)
PSYCHOTIC DISORDER ( 1 FDA reports)
PULMONARY OEDEMA ( 1 FDA reports)
RASH ERYTHEMATOUS ( 1 FDA reports)
RASH GENERALISED ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
REACTION TO DRUG EXCIPIENTS ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE IV ( 1 FDA reports)
RENAL FAILURE ACUTE ( 1 FDA reports)
RENAL IMPAIRMENT ( 1 FDA reports)
RENAL TRANSPLANT ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY FAILURE ( 1 FDA reports)
RHINORRHOEA ( 1 FDA reports)
SALIVA DISCOLOURATION ( 1 FDA reports)
SCAR ( 1 FDA reports)
SCIATICA ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCRATCH ( 1 FDA reports)
SEDATION ( 1 FDA reports)
SELF INJURIOUS BEHAVIOUR ( 1 FDA reports)
SEPSIS ( 1 FDA reports)
SHOULDER OPERATION ( 1 FDA reports)
SKIN DISCOLOURATION ( 1 FDA reports)
SLEEP TERROR ( 1 FDA reports)
SLUGGISHNESS ( 1 FDA reports)
SNEEZING ( 1 FDA reports)
SPEECH DISORDER ( 1 FDA reports)
SPINAL COLUMN STENOSIS ( 1 FDA reports)
STOMATITIS ( 1 FDA reports)
STRESS FRACTURE ( 1 FDA reports)
SUBARACHNOID HAEMORRHAGE ( 1 FDA reports)
SUBSTANCE ABUSE ( 1 FDA reports)
SUDDEN DEATH ( 1 FDA reports)
SUICIDAL BEHAVIOUR ( 1 FDA reports)
SWELLING FACE ( 1 FDA reports)
TENDON DISORDER ( 1 FDA reports)
THERMAL BURN ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
TOBACCO USER ( 1 FDA reports)
TOOTH DISORDER ( 1 FDA reports)
TOOTHACHE ( 1 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 1 FDA reports)
TRAUMATIC FRACTURE ( 1 FDA reports)
TRICHORRHEXIS ( 1 FDA reports)
UNRESPONSIVE TO STIMULI ( 1 FDA reports)
URETHRAL DISORDER ( 1 FDA reports)
URINARY INCONTINENCE ( 1 FDA reports)
URINARY TRACT INFECTION ( 1 FDA reports)
URINE LEUKOCYTE ESTERASE POSITIVE ( 1 FDA reports)
URTICARIA ( 1 FDA reports)
VERTIGO POSITIONAL ( 1 FDA reports)
VISUAL IMPAIRMENT ( 1 FDA reports)
VITAMIN D DECREASED ( 1 FDA reports)
VITREOUS FLOATERS ( 1 FDA reports)
WEIGHT FLUCTUATION ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 1 FDA reports)
WHITE BLOOD CELLS URINE POSITIVE ( 1 FDA reports)
WOUND SECRETION ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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